97-30959. Lambda-Cyhalothrin; Pesticide Tolerance  

  • [Federal Register Volume 62, Number 228 (Wednesday, November 26, 1997)]
    [Rules and Regulations]
    [Pages 63002-63010]
    From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
    [FR Doc No: 97-30959]
    
    
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    ENVIRONMENTAL PROTECTION AGENCY
    
    40 CFR Parts 180, 185 and 186
    
    [OPP-300581; FRL-5755-5]
    RIN 2070-AB78
    
    
    Lambda-Cyhalothrin; Pesticide Tolerance
    
    AGENCY: Environmental Protection Agency (EPA).
    
    ACTION: Final rule.
    
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    SUMMARY: This regulation establishes tolerances for the combined 
    residues of the pyrethroid lambda-cyhalothrin and its epimer in or on 
    broccoli, cabbage, corn (grain, fodder and forage), corn (sweet), 
    cottonseed, dry bulb onion, garlic, lettuce, head, peanuts, rice, 
    soybeans, sorghum, sunflower, tomatoes, wheat, sunflower, and livestock 
    commodities. It also removes time limitations for tolerances for 
    residues of lambda-cyhalothrin on the same commodities that expire on 
    November 15, 1997. The Zeneca Ag Products requested these tolerances 
    under the Federal Food, Drug and Cosmetic Act, as amended by the Food 
    Quality Protection Act of 1996 (Pub. L. 104-170).
    
    DATES: This regulation is effective November 26, 1997. Objections and 
    requests for hearings must be received by EPA on or before January 28, 
    1998.
    
    ADDRESSES: Written objections and hearing requests, identified by the 
    docket control number, [OPP-300581], must be submitted to: Hearing 
    Clerk (1900), Environmental Protection Agency, Rm. M3708, 401 M St., 
    SW., Washington, DC 20460. Fees accompanying objections and hearing 
    requests shall be labeled ``Tolerance Petition Fees'' and forwarded to: 
    EPA Headquarters Accounting Operations Branch, OPP (Tolerance Fees), 
    P.O. Box 360277M, Pittsburgh, PA 15251. A copy of any objections and 
    hearing requests filed with the Hearing Clerk identified by the docket 
    control number, [OPP-300581], must also be submitted to: Public 
    Information and Records Integrity Branch, Information Resources and 
    Services Division (7502C), Office of Pesticide Programs, Environmental 
    Protection Agency, 401 M St., SW., Washington, DC 20460. In person, 
    bring a copy of objections and hearing requests to Rm. 1132, CM #2, 
    1921 Jefferson Davis Hwy., Arlington, VA.
        A copy of objections and hearing requests filed with the Hearing 
    Clerk may also be submitted electronically by sending electronic mail 
    (e-mail) to: opp-docket@epamail.epa.gov. Copies of objections and 
    hearing requests must be submitted as an ASCII file avoiding the use of 
    special characters and any form of encryption. Copies of objections and 
    hearing requests will also be accepted on disks in WordPerfect 5.1/6.1 
    or ASCII file format. All copies of objections and hearing requests in 
    electronic form must be identified by the docket control number [OPP-
    300581]. No Confidential Business Information (CBI) should be submitted 
    through e-mail. Electronic copies of objections and hearing requests on 
    this rule may be filed online at many Federal Depository Libraries.
    
    FOR FURTHER INFORMATION CONTACT: By mail: Adam Heyward, Registration 
    Division (7505C), Office of Pesticide Programs, Environmental 
    Protection Agency, 401 M St., SW., Washington, DC 20460. Office 
    location, telephone number, and e-mail address: Crystal Mall #2, 1921 
    Jefferson Davis Hwy., Arlington, VA, (703) 308-6100, e-mail: 
    heyward.adam@epamail.epa.gov.
    SUPPLEMENTARY INFORMATION: On May 24, 1988, EPA established a time 
    limited tolerance under section 408 of the FFDCA, 21 U.S.C. 346 a(d) 
    and 348 for residues of lambda-cyhalothrin and its epimer on cottonseed 
    (53 FR 18558). As additional crops tolerances were established, they 
    were also made time-limited. These tolerance expire on November 15, 
    1997. Zeneca Ag Products, on September 15, 1997, requested that the 
    time limitation for tolerances for residues of the insecticide lambda-
    cyhalothrin and its epimer in or on the commodities mentioned above be 
    removed based on environmental effects data that they had submitted as 
    a condition of registration. Zeneca Ag Products also submitted a 
    summary of its petition as required under the FFDCA as amended by the 
    Food Quality Protection Act (FQPA) of 1996 (Pub. L. 104-170).
        In the Federal Register of Friday, September 25, 1997 (62 FR 50337) 
    (FRL-5748-2), EPA issued a notice pursuant to section 408 of the 
    Federal Food, Drug, and Cosmetic Act (FFDCA), 21 U.S.C. 346a(e) 
    announcing the filing of pesticide petitions (PP 6F3318, 7F3560, 
    7H5543, 7F3488, 1F3952, 1H5607, 1F3992, 2F4109, 2F4100, 2F4114, 1F3985, 
    9F3770 and 6F4769) for tolerances by Zeneca Ag Products, 1800 Concord 
    Pike, P.O. Box 15458, Wilmington, Delaware 19850-5458. This notice 
    included a summary of the petition prepared by Zeneca Ag Products, the 
    registrant. There were no comments received in response to the notice 
    of filing.
        The petitions requested that 40 CFR 180.438 be amended by removing 
    time limitatioins for tolerances for the combined residue of the 
    insecticide, lambda-cyhalothrin and its epimer in or on the following 
    crops and commodities: broccoli at 0.4 parts per millions (ppm); 
    cabbage at 0.4 ppm; cattle, fat at 3.0 ppm; cattle, meat at 0.2 ppm; 
    cattle, meat and meat by-products (mbyp) at 0.2 ppm; corn, grain (field 
    and pop) at 0.05 ppm; corn, fodder at 1.0 ppm; corn, forage at 6.0 ppm; 
    corn, sweet (k+kwhr) at 0.05 ppm; cottonseed at 0.05 ppm; dry bulb 
    onion at 0.1 ppm; eggs at 0.01 ppm; garlic at 0.1 ppm; goats, fat at 
    3.0 ppm; goats, meat at 0.2 ppm; goats, mbyp at 0.2 ppm, hogs, fat at 
    3.0 ppm; hogs, meat at 0.2 ppm; hogs, mbyp at 0.2 ppm; horses, fat at 
    3.0 ppm; horses, meat at 0.2 ppm; horses, mbyp at 0.2 ppm; lettuce, 
    head at 2.0 ppm; milk, fat (reflecting 0.2 ppm in whole milk) at 5.0 
    ppm; peanuts at 0.05 ppm; peanuts, hulls at 0.05 ppm; poultry, fat at 
    0.01 ppm; poultry, meat at 0.01 ppm; poultry, mbyp at 0.01 ppm; rice, 
    grain at 1.0 ppm; rice, hulls at 5.0 ppm; rice, straw at 1.8 ppm; 
    sheep, fat at 3.0 ppm; sheep, meat at 0.2 ppm; sheep, mbyp at 0.2 ppm; 
    soybeans at 0.01 ppm; sorghum, grain at 0.02 ppm; sorghum, grain dust 
    at 1.5 ppm; sunflower, seeds at 0.2 ppm; sunflower, forage at 0.2 ppm; 
    tomatoes at 0.1 ppm; wheat, grain at 0.05 ppm; wheat, forage at 2.0 
    ppm; wheat, hay at 2.0 ppm; wheat, straw at 2.0 ppm; wheat, grain dust 
    at 2.0 ppm; corn, grain flour at 0.15 ppm; sunflower, oil at 0.30 ppm; 
    sunflower, hulls at 0.50 ppm; tomato pomace (dry or wet) at 6.0 ppm; 
    and wheat, bran at 0.2 ppm.
        In the Notice of Filing the established tolerance level for sorghum 
    grain was inadvertently listed as 0.02 ppm. The correct tolerance level 
    for this commodity if 0.2 ppm. The correct tolerance was considered by 
    EPA for risk assessment purposes. In the latest CFR, 40 CFR 180.438 
    (revised as of July 1, 1997), the tolerance for garlic was incorrectly 
    listed as 0.02 ppm. The correct level if 0.1 ppm. This error occurred 
    when the CFR was updated. The 0.1 ppm level was considered by EPA for 
    risk assessment.
        The basis for time limited tolerances that expire November 15, 1997 
    was given in the October 20, 1993 Federal Register (58 FR 54094). These 
    time-limited tolerances were predicated on the expiration of pesticide 
    product registrations that were made conditional
    
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    due to lack of certain environmental effects data. The rational for 
    using time-limited tolerances was to encourage pesticide manufacturers 
    to comply with the conditions of registration in a timely manner. There 
    is no regulatory requirement to make tolerances time-limited due to the 
    conditional status of a product registration under the Federal 
    Insecticide, Fungicide, Rodenticide Act (FIFRA) as amended. It is 
    current EPA policy to no longer establish time limitations on 
    tolerance(s) if none of the conditions of registration had any bearing 
    on human dietary risk. The current petition action meets that condition 
    and thus the expiration dates associated with specific crop tolerances 
    are being deleted.
    
    I. Risk Assessment and Statutory Findings
    
        New section 408(b)(2)(A)(i) of the FFDCA allows EPA to establish a 
    tolerance (the legal limit for a pesticide chemical residue in or on a 
    food) only if EPA determines that the tolerance is ``safe.'' Section 
    408(b)(2)(A)(ii) defines ``safe'' to mean that ``there is a reasonable 
    certainty that no harm will result from aggregate exposure to the 
    pesticide chemical residue, including all anticipated dietary exposures 
    and all other exposures for which there is reliable information.'' This 
    includes exposure through drinking water and in residential settings, 
    but does not include occupational exposure. Section 408(b)(2)(C) 
    requires EPA to give special consideration to exposure of infants and 
    children to the pesticide chemical residue in establishing a tolerance 
    and to ``ensure that there is a reasonable certainty that no harm will 
    result to infants and children from aggregate exposure to the pesticide 
    chemical residue....''
        EPA performs a number of analyses to determine the risks from 
    aggregate exposure to pesticide residues. First, EPA determines the 
    toxicity of pesticides based primarily on toxicological studies using 
    laboratory animals. These studies address many adverse health effects, 
    including (but not limited to) reproductive effects, developmental 
    toxicity, toxicity to the nervous system, and carcinogenicity. Second, 
    EPA examines exposure to the pesticide through the diet (e.g., food and 
    drinking water) and through exposures that occur as a result of 
    pesticide use in residential settings.
    
    A. Toxicity
    
        1. Threshold and non-threshold effects. For many animal studies, a 
    dose response relationship can be determined, which provides a dose 
    that causes adverse effects (threshold effects) and doses causing no 
    observed effects (the ``no-observed effect level'' or ``NOEL'').
        Once a study has been evaluated and the observed effects have been 
    determined to be threshold effects, EPA generally divides the NOEL from 
    the study with the lowest NOEL by an uncertainty factor (usually 100 or 
    more) to determine the Reference Dose (RfD). The RfD is a level at or 
    below which daily aggregate exposure over a lifetime will not pose 
    appreciable risks to human health. An uncertainty factor (sometimes 
    called a ``safety factor'') of 100 is commonly used since it is assumed 
    that people may be up to 10 times more sensitive to pesticides than the 
    test animals, and that one person or subgroup of the population (such 
    as infants and children) could be up to 10 times more sensitive to a 
    pesticide than another. In addition, EPA assesses the potential risks 
    to infants and children based on the weight of the evidence of the 
    toxicology studies and determines whether an additional uncertainty 
    factor is warranted. Thus, an aggregate daily exposure to a pesticide 
    residue at or below the RfD (expressed as 100 percent or less of the 
    RfD) is generally considered acceptable by EPA. EPA generally uses the 
    RfD to evaluate the chronic risks posed by pesticide exposure. For 
    shorter term risks, EPA calculates a margin of exposure (MOE) by 
    dividing the estimated human exposure into the NOEL from the 
    appropriate animal study. Commonly, EPA finds MOEs lower than 100 to be 
    unacceptable. This hundredfold MOE is based on the same rationale as 
    the hundredfold uncertainty factor.
        Lifetime feeding studies in two species of laboratory animals are 
    conducted to screen pesticides for cancer effects. When evidence of 
    increased cancer is noted in these studies, the Agency conducts a 
    weight of the evidence review of all relevant toxicological data 
    including short-term and mutagenicity studies and structure activity 
    relationship. Once a pesticide has been classified as a potential human 
    carcinogen, different types of risk assessments (e.g., linear low dose 
    extrapolations or MOE calculation based on the appropriate NOEL) will 
    be carried out based on the nature of the carcinogenic response and the 
    Agency's knowledge of its mode of action.
        2. Differences in toxic effect due to exposure duration. The 
    toxicological effects of a pesticide can vary with different exposure 
    durations. EPA considers the entire toxicity data base, and based on 
    the effects seen for different durations and routes of exposure, 
    determines which risk assessments should be done to assure that the 
    public is adequately protected from any pesticide exposure scenario. 
    Both short and long durations of exposure are always considered. 
    Typically, risk assessments include ``acute,'' ``short-term,'' 
    ``intermediate term,'' and ``chronic'' risks. These assessments are 
    defined by the Agency as follows.
        Acute risk, by the Agency's definition, results from 1-day 
    consumption of food and water, and reflects toxicity which could be 
    expressed following a single oral exposure to the pesticide residues. 
    High end exposure to food and water residues are typically assumed.
        Short-term risk results from exposure to the pesticide for a period 
    of 1-7 days, and therefore overlaps with the acute risk assessment. 
    Historically, this risk assessment was intended to address primarily 
    dermal and inhalation exposure which could result, for example, from 
    residential pesticide applications. However, since enaction of FQPA, 
    this assessment has been expanded to include both dietary and non-
    dietary sources of exposure, and will typically consider exposure from 
    food, water, and residential uses when reliable data are available. In 
    this assessment, risks from average food and water exposure, and high-
    end residential exposure, are aggregated. High-end exposures from all 
    three sources are not typically added because of the very low 
    probability of this occurring in most cases, and because the other 
    conservative assumptions built into the assessment assure adequate 
    protection of public health. However, for cases in which high-end 
    exposure can reasonably be expected from multiple sources (e.g. 
    frequent and widespread homeowner use in a specific geographical area), 
    multiple high-end risks will be aggregated and presented as part of the 
    comprehensive risk assessment/characterization. Since the toxicological 
    endpoint considered in this assessment reflects exposure over a period 
    of at least 7 days, an additional degree of conservatism is built into 
    the assessment; i.e., the risk assessment nominally covers 1-7 days 
    exposure, and the toxicological endpoint/NOEL is selected to be 
    adequate for at least 7 days of exposure. (Toxicity results at lower 
    levels when the dosing duration is increased.)
        Intermediate-term risk results from exposure for 7 days to several 
    months. This assessment is handled in a manner similar to the short-
    term risk assessment.
        Chronic risk assessment describes risk which could result from 
    several months
    
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    to a lifetime of exposure. For this assessment, risks are aggregated 
    considering average exposure from all sources for representative 
    population subgroups including infants and children.
    
    B. Aggregate Exposure
    
        In examining aggregate exposure, FFDCA section 408 requires that 
    EPA take into account available and reliable information concerning 
    exposure from the pesticide residue in the food in question, residues 
    in other foods for which there are tolerances, residues in groundwater 
    or surface water that is consumed as drinking water, and other non-
    occupational exposures through pesticide use in gardens, lawns, or 
    buildings (residential and other indoor uses). Dietary exposure to 
    residues of a pesticide in a food commodity are estimated by 
    multiplying the average daily consumption of the food forms of that 
    commodity by the tolerance level or the anticipated pesticide residue 
    level. The Theoretical Maximum Residue Contribution (TMRC) is an 
    estimate of the level of residues consumed daily if each food item 
    contained pesticide residues equal to the tolerance. In evaluating food 
    exposures, EPA takes into account varying consumption patterns of major 
    identifiable subgroups of consumers, including infants and children. 
    The TMRC is a ``worst case'' estimate since it is based on the 
    assumptions that food contains pesticide residues at the tolerance 
    level and that 100% of the crop is treated by pesticides that have 
    established tolerances. If the TMRC exceeds the RfD or poses a lifetime 
    cancer risk that is greater than approximately one in a million, EPA 
    attempts to derive a more accurate exposure estimate for the pesticide 
    by evaluating additional types of information (anticipated residue data 
    and/or percent of crop treated data) which show, generally, that 
    pesticide residues in most foods when they are eaten are well below 
    established tolerances.
    
    II. Aggregate Risk Assessment and Determination of Safety
    
        Consistent with section 408(b)(2)(D), EPA has reviewed the 
    available scientific data and other relevant information in support of 
    this action. EPA has sufficient data to assess the hazards of lambda-
    cyhalothrin and its epimer, and to make a determination on aggregate 
    exposure, consistent with section 408(b)(2) in or on the crops and 
    commodities listed above under SUPPLEMENTARY INFORMATION. EPA's 
    assessment of the dietary exposures and risks associated with 
    establishing the tolerances follows.
    
    A. Toxicological Profile
    
        EPA has evaluated the available toxicity data and considered its 
    validity, completeness, and reliability as well as the relationship of 
    the results of the studies to human risk. EPA has also considered 
    available information concerning the variability of the sensitivities 
    of major identifiable subgroups of consumers, including infants and 
    children. The nature of the toxic effects caused by lambda-cyhalothrin 
    and its epimer are discussed below. Note that the studies discussed 
    below were conducted using either cyhalothrin or lambda-cyhalothrin. 
    Cyhalothrin and lambda-cyhalothrin are basically the same chemical, the 
    differences are found in their stereo chemistry and the number of 
    isomers in each mixture. Cyhalothrin consists of four stereo isomers in 
    each mixture. Cyhalothrin consists of four steno isomers while lambda-
    cyhalothrin is a mixture of the two iomers. The two lambda-cyhalothrin 
    isomers are contained in cyhalothrin, they represent 40% of the 
    cyhalothrin mixture. The major studies submitted to the Agency were 
    conducted with cyhalothrin. However, these studies are used in support 
    of registration for both mixtures. There is evidence, based on 
    subchronic studies in rats, that the two mixtures are not biologically 
    different with respect to their mammalian toxicity.
        1. Acute toxicity studies with the technical grade of the active 
    ingredient lambda-cyahothrin: oral LD50 in the rat of 79 
    milligrams/kilogram (mg/kg) (males) and 56 mg/kg (females)(Tox Category 
    II), dermal LD50 in the rat of 632 mg/kg (males) and 696 mg/
    kg females (Tox Category II), primary eye irritation study showed mild 
    irritation (Tox Category II) and primary dermal irritation study showed 
    no irritation (Tox Category IV).
        2. The following genotoxicity tests were all negative: a gene 
    mutation assay (Ames), a mouse micronucleus assay, an in vitro 
    cytogenetics assay, and a gene mutation study in mouse lymphoma cells.
        3. In a three-generation reproduction study, rats were fed diets 
    containing cyhalothrin at 0, 10, 30 or 100 ppm (approximately 0, 0.5, 
    1.5 or 5.0 mg/kg/day). Parental toxicity was observed as decreased mean 
    body weight and body weight gain during the premating and gestation 
    periods at 5.0 mg/kg/day. There were no other treatment-related 
    effects. Offspring toxicity was observed as reduced mean pup weight and 
    pup weight gains during lactation, again at 5.0 mg/kg/day. No other 
    treatment-related effects were observed. The reproductive and parental 
    NOELs are 1.5 mg/kg/day and the reproductive and parental LOELs are 5.0 
    mg/kg/day. The developmental NOEL is 5.0 mg/kg/day (highest dose 
    tested).
        4. In a developmental toxicity study, rabbits were given gavage 
    dose levels of cyhalothrin at: 0, 3, 10, 30 mg/kg/day during the 
    gestation period (days 6 through 18). The maternal NOEL was 10 mg/kg/
    day and the maternal LOEL was 30 mg/kg/day based on decreased body 
    weight gain (48% of controls) during the dosing period. The 
    developmental NOEL was 30 mg/kg/day highest dose tested (HDT). No 
    developmental effects were observed.
        5. In a developmental study rats were given gavage dose levels of 
    cyhalothrin at: 0, 5, 10, 15 mg/kg/day during the gestation period 
    (days 6 through 15). The maternal NOEL was 10 mg/kg/day and the 
    maternal LOEL was 15 mg/kg/day based on reduced body weight gain (70% 
    of control) and food consumption (as low as 76%) during the dosing 
    period. The developmental NOEL was greater than 15 mg/kg/day (HDT). No 
    developmental effects were observed.
        6. In a 90-day feeding study in rats, lambda-cyhalothrin was fed at 
    doses of, 0, 10, 50 or 250 ppm (0,0.5, 2.5, 12.5 mg/kg/day). The 
    animals were examined once daily for clinical signs of toxicity. 
    Bodyweights, food consumption, hematological and clinical chemistry 
    parameters, urinalysis parameters, organ weights, and macroscopic and 
    microscopic observations were recorded. Body weight gain and food 
    consumption were significantly reduced for both sexes at 12.5 mg/kg/
    day. There was also a slight but statistically significant reduction in 
    food efficiency in females at this dose level. The NOEL is 2.5 mg/kg/
    day and the LEL is 12.5 mg/kg/day based on reduction in bodyweight gain 
    and food consumption in both sexes and food efficiency in females.
        7. In another 90-day feeding study in rats cyhalothrin was fed at 
    doses of 0, 10, 50 or 250 ppm (0, 0.5, 2.5, 12.5 mg/kg/day). The 
    animals were examined for clinical signs of toxicity. Bodyweights, food 
    consumption, hematological and clinical chemistry parameters, 
    urinalysis parameters, organ weights, and macroscopic and microscopic 
    observations were recorded. Body weight gain was significantly reduced 
    in males at 12.5 mg/kg/day. Body weight gain was also significantly 
    reduced in females at this level, but only during the first week. Body 
    weight gain was not significantly affected at lower dose
    
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    levels. The NOEL is 2.5 mg/kg/day and the LEL is 12.5 mg/kg/day based 
    on decreased bodyweight gain.
        8. A In 28-day study in the mouse cyhalothrin was fed to mice in 
    the diet as a range-finding study for the carcinogenicity study at 0, 
    5, 25, 100, 500, or 2,000 ppm (0, 0.65, 3.30, 13.5, 64.2 or 309 mg/kg/
    day for males and 0, 0.80, 4.17, 15.2, 77.9 or 294 mg/kg/day for 
    females).The NOEL is 500 ppm and the LEL is 2,000 ppm based on 
    mortality, clinical signs of toxicity, decreases in body weight gain 
    and food consumption, changes in hematology and organ weights and 
    minimal centrilobular hepatocyte enlargement.
        9. In a 21 day dermal toxicity study rats were exposed dermally to 
    doses of 1, 10, or 100 mg/kg of lambda-cyhalothrin (reduced to 50 mg/kg 
    after two or three applications) 6 hours/day for 21 consecutive days. 
    No significant signs of skin irritation was observed at any dose level. 
    Two male rats were found dead after 3 applications of 100 mg/kg. There 
    was no evidence prior to death, at postmortem examination, or from 
    histopathology, of the possible cause of death, but it is thought 
    likely to be due to pyrethroid toxicity. Animals dosed with 50 mg/kg/
    day displayed clinical signs of slight general toxicity (bizarre 
    behavior, paw flicking, splayed gait, sides pinched in, thin, tip-toe 
    gait, reduced stability, dehydration and reduced splay reflex). Effects 
    on body weight gain and food consumption were also seen in males at 
    this dose level. No toxicologically significant treatment-related 
    effects were observed at any other dose level. The NOEL is 10 mg/kg/day 
    and the LEL is 100/50 mg/kg/day based on death, clinical signs of 
    toxicity and decreased bodyweight gain and food consumption.
        10. In a 21-day inhalation study rats were exposed nose-only 6 
    hours/day, 5 days/week for 21 days to lambda-cyhalothrin at 0.3, 3.3, 
    or 16.7 g/L. The NOEL was 0.3 g/L and the LOEL was 
    3.3 g/L based on decreased bodyweight gains (high dose males) 
    and food consumption (high dose, both sexes), clinical signs of 
    toxicity (paw flicking, tail erections, tiptoe gait, lachrymation or 
    salivation), punctate foci on cornea (both sexes, mid- and high dose), 
    raised prothrombin time, changes in hematology, clinical chemistry and 
    urinalysis parameters and a slight increase in the incidence of 
    alveolitis in females.
        11. In a 12-month chronic/carcinogenicity feeding study, dogs were 
    fed dose (by capsule) levels of lambda-cyhalothrin at 0, 0.1, 0.5, 3.5 
    mg/kg/day with a NOEL of 0.1 mg/kg/day. The LOEL for this study is 
    established at 0.5 mg/kg/day based upon clinical signs of 
    neurotoxicity.
        12. In a 24-month chronic feeding/carcinogenicity study rats were 
    fed diets containing 0, 10, 50, and 250 ppm (0, 0.5, 2.5 or 12.5 mg/kg/
    day) of cyhalothrin. The LEL for chronic toxicity in rats is 12.5 mg/
    kg/day and the NOEL is 2.5 mg/kg/day. There was no indication of 
    carcinogenic effects observed under the conditions of the study.
        13. In a carcinogenicity study, mice were fed dose levels of 0, 20, 
    100, or 500 ppm (0, 3, 15, or 75 mg/kg/day) of cyhalothrin in the diet 
    for 2 years. A systemic NOEL was established at 100 ppm and systemic 
    LOEL at 500 ppm based on decreased body weight gain in males throughout 
    the study at 500 ppm. The EPA has classified lambda-cyhalothrin as a 
    Group D carcinogen (not classifiable due to an equivocal finding in 
    this study). No treatment-related carcinogenic effects were observed 
    under the conditions of the study.
        14. Metabolism studies in rats demonstrated that distribution 
    patterns and excretion rates in multiple oral dose studies are similar 
    to single-dose studies. Accumulation of unchanged compound in fat upon 
    chronic administration with slow elimination. Otherwise, lambda-
    cyhalothrin was rapidly metabolized and excreted. The metabolism of 
    lambda-cyhalothrin in livestock has been studied in the goat, chicken, 
    and cow.
        15. No neurotoxicity studies are available. These studies will be 
    required under a special data call-in letter pursuant to Section 
    3(c)(2)(B) of FIFRA. Although these data are lacking EPA has sufficient 
    toxicity data to support these tolerances and these additional studies 
    are not expected to significantly change its risk assessment.
    
    B. Toxicological Endpoints
    
        1. Acute toxicity. For acute dietary risk assessment, EPA used a 
    systemic NOEL of 0.5 mg/kg/day based on gait adnormalities in dogs on 
    day 2 in the chronic toxicity study.
        2. Short - and intermediate - term toxicity. For short-and 
    intermediate-term dermal risk assessment, EPA recommends use of a NOEL 
    of 10.0 mg/kg/day from the 21-day dermal toxicity study based on 
    systemic toxicity at 50 mg/kg/day (LOEL). A dermal absorption rate of 
    25% was used based on weight of the evidence available for all 
    structurally related pyrethroids. EPA used a NOEL of 0.3 g/L 
    from the 21-day inhalation study in rats based on clinical signs 
    indicative of neurotoxicity (paw slicking) tail erections, and tiptoe 
    gait) at 3.3 g/L.
        3. Chronic toxicity. EPA has established the reference dose (RfD) 
    for lambda-cyhalothrin at 0.001 mg/kg/day. This RfD is based on a 1-
    year oral study in dogs with a NOEL of 0.1 mg/kg/day and an uncertainty 
    factor (UF) of 100. The LEL of 0.5 mg/kg/day was based on clinical 
    signs of neurotoxicity (convulsions, ataxia, muscle tremors) and a 
    slight increase in liquid feces.
        4. Carcinogenicity. Based on the available carcinogenicity studies 
    in two rodent species, lambda-cyhalothrin has been classified as a 
    Group ``D'' chemical, ``not classifiable as to human carcinogenicity.'' 
    Although lambda-cyhalothrin was not shown to be carcinogenic in either 
    the mouse or rat, the EPA Health Effects Division (HED) RfD/PEER review 
    committee based the ``D'' classification on: (1) Lambda-cyhalothrin was 
    not tested at adequate dose levels for carcinogenicity testing in the 
    mouse, and (2) the equivocal nature of the findings with regard to the 
    incidence of mammary adenocarcinomas. No additional cancer studies are 
    being required at this time.
    
    C. Exposures and Risks
    
        1. From food and feed uses. The primary source of human exposure to 
    lambda-cyhalothrin will be from ingestion of both raw and processed 
    food commodities treated with lambda-cyhalothrin. Tolerances have been 
    established in 40 CFR 180.438 and 40 CFR 186.3765 for combined residues 
    of lambda-cyhalothrin and its epimer in or on a variety of food 
    commodities. Risk assessments were conducted by EPA to assess dietary 
    exposures and risks from lambda-cyhalothrin as follows:
        i. Acute exposure and risk. An acute dietary risk assessments are 
    performed for a food-use pesticide if a toxicological study has 
    indicated the possibility of an effect of concern occurring as a result 
    of a 1 day or single exposure. The acute dietary exposure used Monte 
    Carlo modeling incorporating anticipated residue and percent crop 
    treated refinements. The acute dietary Margin of Exposure (MOE) 
    calculated at the 99.9th percentile for the most highly exposed 
    population subgroup (non-nursing infants < 1="" year="" old)="" is="" 139.="" the="" moe="" calculated="" at="" the="" 99.9th="" percentile="" for="" the="" general="" u.s.="" population="" is="" 311.="" epa="" concludes="" that="" there="" is="" a="" reasonable="" certainty="" of="" no="" harm="" for="" moe="" of="" 100="" or="" greater.="" therefore,="" the="" acute="" dietary="" risk="" assessment="" for="" lambda-cyhalothrin="" indicates="" a="" reasonable="" certainty="" of="" no="" harm.="" ii.="" chronic="" exposure="" and="" risk.="" the="" rfd="" used="" for="" the="" chronic="" dietary="" analysis="" is="" [[page="" 63006]]="" 0.001="" mg/kg/day="" from="" the="" lambda-cyhalothrin="" chronic="" dog="" study="" and="" an="" uncertainty="" factor="" of="" 100.="" the="" chronic="" dietary="" exposure="" assessment="" used="" anticipated="" residues="" and="" percent="" crop="" treated="" information.="" the="" chronic="" dietary="" exposure="" estimate="" for="" the="" overall="" u.s.="" population="" was="" calculated="" to="" be="" 0.000068="" mg/kg/day="" (6.8%="" of="" the="" rfd="" utilized)="" and="" for="" children="" 1-6="" years="" was="" calculated="" to="" be="" 0.000192="" mg/kg/day="" (19.2%="" of="" the="" rfd="" utilized).="" epa="" notes="" that="" the="" acute="" dietary="" risk="" assessments="" used="" monte="" carlo="" modeling="" (in="" accordance="" with="" tier="" 3="" of="" epa="" june="" 1996="" ``acute="" dietary="" exposure="" assessment''="" guidance="" document)="" incorporating="" anticipated="" residues="" and="" percent="" crop="" treated="" refinements.="" the="" chronic="" dietary="" risk="" assessment="" used="" percent="" crop="" treated="" information="" and="" anticipated="" residues.="" section="" 408(b)(2)(e)="" authorizes="" epa="" to="" consider="" available="" data="" and="" information="" on="" the="" antipicated="" residue="" levels="" of="" pesticide="" chemicals="" that="" have="" been="" measure="" in="" food.="" if="" epa="" relies="" on="" such="" information,="" epa="" must="" require="" that="" data="" be="" provided="" 5="" years="" after="" the="" tolerance="" is="" established,="" modified="" or="" left="" in="" effect,="" demonstration="" that="" the="" levels="" in="" food="" are="" not="" above="" the="" levels="" anticipated.="" following="" the="" initial="" data="" submission,="" epa="" is="" authorized="" to="" require="" similar="" data="" on="" a="" timeframe="" it="" deems="" appropriate.="" section="" 408="" (b)(2)(f)="" allows="" the="" agency="" to="" use="" data="" on="" the="" actual="" percent="" of="" crop="" treated="" when="" establishing="" a="" tolerance="" only="" where="" the="" agency="" can="" make="" the="" following="" findings:="" (1)="" that="" the="" data="" used="" are="" reliable="" and="" provide="" a="" valid="" basis="" for="" showing="" the="" percentage="" of="" food="" derived="" from="" a="" crop="" that="" is="" likely="" to="" contain="" residues;="" (2)="" that="" the="" exposure="" estimate="" does="" not="" underestimate="" the="" exposure="" for="" any="" significant="" subpopulation="" and;="" (3)="" where="" data="" on="" regional="" pesticide="" use="" and="" food="" consumption="" are="" available,="" that="" the="" exposure="" estimate="" does="" not="" understate="" exposure="" for="" any="" regional="" population.="" in="" addition,="" the="" agency="" must="" provide="" for="" periodic="" evaluation="" of="" any="" estimates="" used.="" the="" percent="" of="" crop="" treated="" estimates="" for="" lambda-cyhalothrin="" were="" derived="" from="" federal="" and="" market="" survey="" data.="" epa="" considers="" these="" reliable.="" a="" range="" of="" estimates="" are="" supplied="" by="" this="" data="" and="" the="" upper="" end="" of="" this="" range="" was="" used="" for="" the="" exposure="" assessment.="" by="" using="" this="" upper="" end="" estimate="" of="" percent="" of="" crop="" treated,="" the="" agency="" is="" reasonably="" certain="" that="" exposure="" is="" not="" understated="" for="" any="" significant="" subpopulation="" group.="" further,="" regional="" consumption="" information="" is="" taken="" into="" account="" through="" epa's="" computer-based="" model="" for="" evaluating="" the="" exposure="" of="" significant="" subpopulations="" including="" several="" regional="" groups.="" review="" of="" this="" regional="" data="" allows="" the="" agency="" to="" be="" reasonably="" certain="" that="" no="" regional="" population="" is="" exposed="" to="" residue="" levels="" higher="" than="" those="" estimated="" by="" the="" agency.="" to="" meet="" the="" requirement="" for="" data="" on="" anticipated="" residues,="" epa="" will="" issue="" a="" date="" call-in="" (dci)="" notice="" pursuant="" to="" ffdca="" section="" 408(f)="" requiring="" submission="" of="" data="" on="" anticipated="" residues="" in="" conjunction="" with="" approval="" of="" the="" registration="" under="" the="" fifra.="" 2.="" from="" drinking="" water.="" laboratory="" and="" field="" data="" have="" demonstrated="" that="" lambda-cyhalothrin="" is="" immobile="" in="" soil="" and="" will="" not="" leach="" into="" groundwater.="" other="" data="" show="" that="" lambda-cyhalothrin="" is="" virtually="" insoluble="" in="" water="" and="" extremely="" lipophilic.="" as="" a="" result,="" epa="" concludes="" that="" residues="" reaching="" surface="" waters="" from="" field="" runoff="" will="" quickly="" adsorb="" to="" sediment="" particles="" and="" be="" partitioned="" from="" the="" water="" column.="" further,="" a="" screening="" evaluation="" of="" leaching="" potential="" of="" a="" typical="" pyrethroid="" was="" conducted="" using="" epa's="" pesticide="" root="" zone="" model="" (przm1).="" based="" on="" this="" screening="" assessment,="" the="" potential="" concentrations="" of="" a="" pyrethroid="" in="" groundwater="" at="" depths="" of="" 1="" and="" 2="" meters="" are="" essentially="" zero=""><0.001 parts="" per="" billion="" (ppb)).="" surface="" water="" concentrations="" for="" pyrethroids="" were="" estimated="" using="" przm3="" and="" exposure="" analysis="" modeling="" system="" (exams)="" using="" standard="" epa="" cotton="" runoff="" and="" mississippi="" pond="" scenarios.="" the="" maximum="" concentration="" predicted="" in="" the="" simulated="" pond="" was="" 0.052="" ppb.="" concentrations="" in="" actual="" drinking="" water="" would="" be="" much="" lower="" than="" the="" levels="" predicted="" in="" the="" hypothetical,="" small,="" stagnant="" farm="" pond="" model="" since="" drinking="" water="" derived="" from="" surface="" water="" would="" normally="" be="" treated="" before="" consumption.="" i.="" acute="" exposure="" and="" risk.="" the="" acute="" drinking="" water="" exposure="" and="" risk="" estimates="" are="" 0.000022="" mg/kg/day="" (moe="" 22,876)="" and="" 0.000042="" mg/kg/="" day="" (moe="" 11,956)="" for="" the="" overall="" u.s.="" population="" and="" non-nursing="" infants="">< 1="" year="" old,="" respectively.="" ii.="" chronic="" exposure="" and="" risk.="" the="" chronic="" drinking="" water="" exposure="" and="" risk="" estimates="" are="" 0.000000="" mg/kg/day="" (0.0%="" of="" rfd="" utilized)="" and="" 0.000000="" mg/kg/day="" (0.0%="" of="" rfd.="" utilized)="" for="" the="" overall="" u.s.="" population="" and="" non-nursing="" infants="">< 1="" year="" old,="" respectively.="" 3.="" from="" non-dietary="" exposure.="" lambda-cyhalothrin="" is="" currently="" registered="" for="" use="" on="" the="" following="" residential="" non-food="" sites:="" general="" indoor/outdoor="" pest="" control="" (crack/crevice/spot),="" termiticide,="" ornamental="" plants="" and="" lawns="" around="" homes,="" parks,="" recreation="" areas="" and="" athletic="" fields,="" and="" golf="" course="" turf.="" application="" of="" this="" pesticide="" in="" and="" around="" these="" sites="" is="" mainly="" limited="" to="" commercial="" applicators.="" analyses="" were="" conducted="" which="" included="" an="" evaluation="" of="" potential="" non-="" dietary="" (residential)="" applicator,="" post-application="" and="" chronic="" dietary="" aggregate="" exposures="" associated="" with="" lambda-cyhalothrin="" products="" used="" for="" residential="" flea="" infestation="" control="" and="" agricultural/commercial="" applications.="" in="" the="" case="" of="" potential="" non-dietary="" health="" risks,="" conservative="" point="" estimates="" of="" non-dietary="" exposures,="" expressed="" as="" total="" systemic="" absorbed="" dose="" (summed="" across="" inhalation="" and="" incidental="" ingestion="" routes)="" for="" each="" relevant="" product="" use="" category="" (i.e.="" lawn="" care)="" and="" receptor="" based="" on="" the="" toxicity="" endpoints="" selected="" by="" epa="" for="" lambda-cyhalothrin,="" inhalation="" and="" incidental="" oral="" ingestion="" absorbed="" doses="" were="" combined="" and="" compared="" to="" the="" relevant="" systemic="" noel="" for="" estimating="" moes.="" 4.="" short-="" and="" intermediate-term="" exposure="" and="" risk.="" epa="" used="" a="" noel="" of="" 0.3="">g/L (0.05 mg/kg/day) from the 21-day inhalation 
    toxicity study in rats. The LOEL of 3.3 g/L was based on 
    decreased body weight gains and clinical signs of toxicity including 
    paw flicking, tail erections and tiptoe gait. For short- and 
    intermediate-term dermal exposure MOE calculations, EPA used a NOEL of 
    10.0 mg/kg/day based on systemic toxicity at 50 mg/kg/day (LOEL). MOE = 
    100.
        The short and intermediate-term non-dietary aggregate (non-dietary 
    + chronic dietary (food and water)) MOEs for lambda-cyhalothrin 
    indicate a substantial degree of safety. The total non-dietary 
    (inhalation + incidental ingestion + dermal) MOEs for post-application 
    exposure for the lawn care product evaluated was estimated to be > 
    15,000 for adults, 7,200 for children 1-6 years old and 7,000 for 
    infants < 1="" year.="" it="" can="" be="" concluded="" that="" the="" potential="" non-dietary="" and="" aggregate="" (non-dietary="" +="" chronic="" dietary)="" exposures="" for="" lambda-="" cyhalothrin="" are="" associated="" with="" substantial="" margin="" of="" safety.="" 5.="" cumulative="" exposure="" to="" substances="" with="" common="" mechanism="" of="" toxicity.="" section="" 408(b)(2)(d)(v)="" requires="" that,="" when="" considering="" whether="" to="" establish,="" modify,="" or="" revoke="" a="" tolerance,="" the="" agency="" consider="" ``available="" information''="" concerning="" the="" cumulative="" effects="" of="" a="" particular="" pesticide's="" residues="" and="" ``other="" substances="" that="" have="" a="" common="" mechanism="" of="" toxicity.''="" the="" agency="" believes="" that="" ``available="" information''="" in="" this="" context="" might="" include="" not="" only="" toxicity,="" chemistry,="" [[page="" 63007]]="" and="" exposure="" data,="" but="" also="" scientific="" policies="" and="" methodologies="" for="" understanding="" common="" mechanisms="" of="" toxicity="" and="" conducting="" cumulative="" risk="" assessments.="" for="" most="" pesticides,="" although="" the="" agency="" has="" some="" information="" in="" its="" files="" that="" may="" turn="" out="" to="" be="" helpful="" in="" eventually="" determining="" whether="" a="" pesticide="" shares="" a="" common="" mechanism="" of="" toxicity="" with="" any="" other="" substances,="" epa="" does="" not="" at="" this="" time="" have="" the="" methodologies="" to="" resolve="" the="" complex="" scientific="" issues="" concerning="" common="" mechanism="" of="" toxicity="" in="" a="" meaningful="" way.="" epa="" has="" begun="" a="" pilot="" process="" to="" study="" this="" issue="" further="" through="" the="" examination="" of="" particular="" classes="" of="" pesticides.="" the="" agency="" hopes="" that="" the="" results="" of="" this="" pilot="" process="" will="" increase="" the="" agency's="" scientific="" understanding="" of="" this="" question="" such="" that="" epa="" will="" be="" able="" to="" develop="" and="" apply="" scientific="" principles="" for="" better="" determining="" which="" chemicals="" have="" a="" common="" mechanism="" of="" toxicity="" and="" evaluating="" the="" cumulative="" effects="" of="" such="" chemicals.="" the="" agency="" anticipates,="" however,="" that="" even="" as="" its="" understanding="" of="" the="" science="" of="" common="" mechanisms="" increases,="" decisions="" on="" specific="" classes="" of="" chemicals="" will="" be="" heavily="" dependent="" on="" chemical="" specific="" data,="" much="" of="" which="" may="" not="" be="" presently="" available.="" although="" at="" present="" the="" agency="" does="" not="" know="" how="" to="" apply="" the="" information="" in="" its="" files="" concerning="" common="" mechanism="" issues="" to="" most="" risk="" assessments,="" there="" are="" pesticides="" as="" to="" which="" the="" common="" mechanism="" issues="" can="" be="" resolved.="" these="" pesticides="" include="" pesticides="" that="" are="" toxicologically="" dissimilar="" to="" existing="" chemical="" substances="" (in="" which="" case="" the="" agency="" can="" conclude="" that="" it="" is="" unlikely="" that="" a="" pesticide="" shares="" a="" common="" mechanism="" of="" activity="" with="" other="" substances)="" and="" pesticides="" that="" produce="" a="" common="" toxic="" metabolite="" (in="" which="" case="" common="" mechanism="" of="" activity="" will="" be="" assumed).="" although="" lambda-cyhalothrin="" is="" structurally="" similar="" to="" other="" members="" of="" the="" synthetic="" pyrethroids="" class="" of="" insecticide,="" epa="" does="" not="" have,="" at="" this="" time,="" available="" data="" to="" determine="" whether="" lambda-="" cyhalothrin="" has="" a="" common="" mechanism="" of="" toxicity="" with="" other="" substances="" or="" how="" to="" include="" this="" pesticide="" in="" a="" cumulative="" risk="" assessment.="" unlike="" other="" pesticides="" for="" which="" epa="" has="" followed="" a="" cumulative="" risk="" approach="" based="" on="" a="" common="" mechanism="" of="" toxicity,="" lambda-cyhalothrin="" does="" not="" appear="" to="" produce="" a="" toxic="" metabolite="" produced="" by="" other="" substances.="" for="" the="" purposes="" of="" this="" tolerance="" action,="" therefore,="" epa="" has="" not="" assumed="" that="" lambda-cyhalothrin="" has="" a="" common="" mechanism="" of="" toxicity="" with="" other="" substances.="" d.="" aggregate="" risks="" and="" determination="" of="" safety="" for="" u.s.="" population="" 1.="" acute="" risk.="" the="" acute="" aggregate="" risk="" assessment="" takes="" into="" account="" exposure="" from="" food="" and="" water.="" the="" acute="" aggregate="" moe="" calculated="" at="" the="" 99.th="" percentile="" for="" the="" u.s.="" population="" is="" 307.="" in="" a="" conservative="" policy,="" the="" agency="" has="" no="" cause="" for="" concern="" if="" total="" acute="" exposure="" calculated="" for="" the="" 99.9th="" percentile="" yields="" a="" moe="" of="" 100="" or="" large.="" epa="" concludes="" that="" there="" is="" a="" reasonable="" certainty="" that="" no="" harm="" will="" result="" from="" acute="" aggregate="" exposure="" to="" lambda-cyhalothrin="" residues.="" 2.="" chronic="" risk.="" aggregate="" chronic="" exposure="" is="" the="" sum="" of="" chronic="" exposure="" from="" food="" and="" chronic="" water.="" using="" the="" exposure="" assumptions="" described="" above,="" epa="" has="" concluded="" that="" aggregate="" exposure="" to="" lambda-="" cyhalothrin="" from="" food="" and="" water="" will="" utilize="" 6.8%="" of="" the="" rfd="" for="" the="" u.s.="" population.="" epa="" generally="" has="" no="" concern="" for="" exposures="" below="" 100%="" of="" the="" rfd="" because="" the="" rfd="" represents="" the="" level="" at="" or="" below="" which="" daily="" aggregate="" dietary="" exposure="" over="" a="" lifetime="" will="" not="" pose="" appreciable="" risks="" to="" human="" health..="" epa="" concludes="" that="" there="" is="" a="" reasonable="" certainty="" that="" no="" harm="" will="" result="" from="" chronic="" aggregate="" exposure="" to="" lambda-cyhalothrin="" residues.="" 3.="" short-="" and="" intermediate-term="" risk..="" short-="" and="" intermediate-="" term="" aggregate="" exposure="" takes="" into="" account="" chronic="" dietary="" food="" and="" water="" (considered="" to="" be="" a="" background="" exposure="" level)="" plus="" indoor="" and="" outdoor="" residential="" exposure.="" for="" lambda-cyhalothrin="" the="" aggegrate="" moe="" (inhalation="" +="" incidental="" oral="" +="" chronic="" dietary="" summed="" across="" all="" product="" use="" category="" was="" estimated="" to="" be="" 14,000="" for="" the="" u.s.="" population.="" epa="" concludes="" that="" the="" aggregate="" short-="" and="" intermediate-="" term="" risks="" do="" not="" exceed="" levels="" of="" concern,="" and="" that="" there="" is="" reasonable="" certainty="" that="" no="" harm="" will="" result="" from="" aggregate="" exposure="" to="" lambda-cyhalothrin="" residues.="" e.="" aggregate="" cancer="" risk="" for="" u.s.="" population="" lambda-cyhalothrin="" has="" been="" classified="" by="" epa="" as="" a="" group="" ``d''="" chemical,="" ``not="" classifiable="" as="" to="" human="" carcinogenicity.''="" therefore,="" this="" risk="" assessment="" was="" not="" conducted.="" f.="" aggregate="" risks="" and="" determination="" of="" safety="" for="" infants="" and="" children="" in="" assessing="" the="" potential="" for="" additional="" sensitivity="" of="" infants="" and="" children="" to="" residues="" of="" lambda-cyhalothrin,="" epa="" considered="" data="" from="" developmental="" toxicity="" studies="" in="" rats="" and="" rabbits="" and="" a="" three-="" generation="" reproductive="" toxicity="" study="" in="" rats.="" the="" developmental="" toxicity="" studies="" are="" designed="" to="" evaluate="" adverse="" effects="" on="" the="" developing="" organism="" resulting="" from="" maternal="" pesticide="" exposure="" during="" prenatal="" development.="" reproduction="" studies="" provide="" information="" relating="" to="" pre-="" and="" post-natal="" effects="" from="" exposure="" to="" the="" pesticide,="" information="" on="" the="" reproductive="" capability="" of="" mating="" animals,="" and="" data="" on="" systemic="" toxicity.="" ffdca="" section="" 408="" provides="" that="" epa="" shall="" apply="" an="" additional="" tenfold="" margin="" of="" safety="" for="" infants="" and="" children="" in="" the="" case="" of="" threshold="" effects="" to="" account="" for="" pre-and="" post-natal="" toxicity="" and="" the="" completeness="" of="" the="" database="" unless="" epa="" determines="" that="" a="" different="" margin="" of="" safety="" will="" be="" safe="" for="" infants="" and="" children.="" margins="" of="" safety="" are="" incorporated="" into="" epa="" risk="" assessments="" either="" directly="" through="" use="" of="" a="" margin="" of="" exposure="" analysis="" or="" through="" using="" uncertainty="" (safety)="" factors="" in="" calculating="" a="" dose="" level="" that="" poses="" no="" appreciable="" risk="" to="" humans.="" in="" either="" case,="" epa="" generally="" defines="" the="" level="" of="" appreciable="" risk="" as="" exposure="" that="" is="" greater="" than="" 1/100="" of="" the="" noel="" in="" the="" animal="" study="" appropriate="" to="" the="" particular="" risk="" assessment.="" this="" hundredfold="" uncertainty="" (safety)="" factor="" is="" designed="" to="" account="" for="" inter-species="" extrapolation="" and="" intra-species="" variability.="" epa="" believes="" that="" reliable="" data="" support="" using="" the="" standard="" hundredfold="" factor="" when="" epa="" has="" a="" complete="" data="" base="" under="" existing="" guidelines="" and="" when="" the="" severity="" of="" the="" effect="" in="" infants="" or="" children="" or="" the="" potency="" or="" unusual="" toxic="" properties="" of="" a="" compound="" do="" not="" raise="" concerns="" regarding="" the="" adequacy="" of="" the="" standard="" factor.="" 1.="" developmental="" toxicity="" studies.="" i.="" from="" the="" developmental="" toxicity="" study="" in="" rats,="" the="" maternal="" (systemic)="" noel="" was="" 10="" mg/kg/day.="" the="" maternal="" lel="" of="" 15="" mg/kg/day="" was="" based="" on="" decreased="" body="" weight="" gain="" and="" decreased="" food="" consumption.="" the="" developmental="" (fetal)="" noel="" was=""> 15 mg/kg/day at the HDT.
        ii. From the developmental toxicity study in rabbits, the maternal 
    (systemic) NOEL was 10 mg/kg/day. The maternal LEL of 30 mg/kg/day was 
    based on decreased body weight gain. The developmental (fetal) NOEL was 
     30 mg/kg/day (HDT).
        2. Reproductive toxicity study. From the three-generation 
    reproductive toxicity study in rats, both the parental (systemic) and 
    reproductive (pup) NOEL's were 1.5 mg/kg/day. Both the parental 
    (systemic) and reproductive (pup) LEL's were 5 mg/kg/day. They were 
    based on a significant decrease in
    
    [[Page 63008]]
    
    parental body weight (systemic) or a significant decrease in pup body.
        3. Pre- and post-natal sensitivity. The toxicology data base for 
    lambda-cyhalothrin is complete with respect to current toxicological 
    data requirements. There are no pre- or post-natal toxicity concerns 
    for infants and children, based on the results of the rat and rabbit 
    developmental toxicity studies and the three-generation reproductive 
    toxicity study in rats.
        The toxicological database relative to pre- and post- natal 
    sensitivity is complete. Based on the above, EPA concludes that 
    reliable data support the use of the standard hundredfold margin of 
    uncertainty factor and that an additional uncertainty factor is not 
    warranted at this time.
        4. Acute risk. The aggregate acute MOE calculated at the 99.9th 
    percentile for non-nursing infants < 1="" year="" old="" is="" 138.="" the="" agency="" has="" no="" cause="" for="" concern="" if="" total="" acute="" exposure="" calculated="" for="" the="" 99.9th="" percentile="" yields="" a="" moe="" of="" 100="" or="" larger.="" therefore,="" the="" agency="" has="" no="" acute="" aggregate="" concern="" due="" to="" exposure="" to="" lambda-cyhalothrin="" through="" food="" and="" drinking="" water.="" 5.="" chronic="" risk.="" using="" the="" conservative="" exposure="" assumptions="" described="" above,="" epa="" has="" concluded="" that="" aggregate="" exposure="" to="" lambda-="" cyhalothrin="" from="" food="" will="" utilize="" 19.2%="" of="" the="" rfd="" for="" children="" 1-6="" years="" old.="" epa="" generally="" has="" no="" concern="" for="" exposures="" below="" 100%="" of="" the="" rfd="" because="" the="" rfd="" represents="" the="" level="" at="" or="" below="" which="" daily="" aggregate="" dietary="" exposure="" over="" a="" lifetime="" will="" not="" pose="" appreciable="" risks="" to="" human="" health.="" epa="" concludes="" that="" there="" is="" a="" reasonable="" certainty="" that="" no="" harm="" will="" result="" to="" infants="" and="" children="" from="" aggregate="" exposure="" to="" lambda-cyhalothrin="" residues.="" 6.="" short-="" and="" intermediate-term="" risk.="" short-="" and="" intermediate-term="" aggregate="" exposure="" takes="" into="" account="" chronic="" dietary="" food="" and="" water="" (considered="" to="" be="" a="" background="" level)="" plus="" short-term="" and="" intermediate="" term="" residential="" exposure.="" the="" aggregate="" moe="" was="" estimated="" to="" be="" 6,300="" for="" children="" 1-6="" years="" old="" and="" 6,800="" for="" infants="">< 1="" year="" old).="" epa="" concludes="" that="" the="" aggregate="" short-="" and="" intermediate-term="" risks="" do="" not="" exceed="" levels="" of="" concern,="" and="" that="" there="" is="" reasonable="" certainty="" that="" no="" harm="" will="" result="" from="" aggregate="" exposure="" to="" lambda-cyhalothrin="" residues.="" g.="" endocrine="" disruption="" epa="" is="" required="" to="" develop="" a="" screening="" program="" to="" determine="" whether="" certain="" substances="" (including="" all="" pesticides="" and="" inerts)="" ``may="" have="" an="" effect="" in="" humans="" that="" is="" similar="" to="" an="" effect="" produced="" by="" a="" naturally="" occurring="" estrogen,="" or="" such="" other="" endocrine="" effect....''="" the="" agency="" is="" currently="" working="" with="" interested="" stakeholders,="" including="" other="" government="" agencies,="" public="" interest="" groups,="" industry="" and="" research="" scientists="" in="" developing="" a="" screening="" and="" testing="" program="" and="" a="" priority="" setting="" scheme="" to="" implement="" this="" program.="" congress="" has="" allowed="" 3="" years="" from="" the="" passage="" of="" fqpa="" (august="" 3,="" 1999)="" to="" implement="" this="" program.="" at="" that="" time,="" epa="" may="" require="" further="" testing="" of="" this="" active="" ingredient="" and="" end="" use="" products="" for="" endocrine="" disrupter="" effects.="" iii.="" other="" considerations="" a.="" metabolism="" in="" plants="" and="" animals="" the="" metabolism="" of="" lambda-cyhalothrin="" in="" plants="" and="" animals="" is="" adequately="" understood="" for="" the="" purpose="" of="" this="" tolerance.="" epa="" has="" determined="" that="" plant="" and="" animal="" metabolites="" do="" not="" need="" to="" appear="" in="" the="" tolerance="" expression="" at="" this="" time.="" the="" residues="" to="" be="" regulated="" are="" lambda-cyhalothrin="" and="" its="" epimer="" as="" specified="" in="" 40="" cfr="" 180.438.="" b.="" analytical="" enforcement="" methodology="" there="" is="" a="" practical="" analytical="" method="" available="" for="" determination="" of="" residues="" of="" lambda-cyhalothrin="" and="" its="" epimer.="" adequate="" enforcement="" methodology="" (gas="" chromatography/electron="" capture="" detector)="" for="" plant="" and="" animal="" commodities="" is="" available="" to="" enforce="" the="" tolerances.="" epa="" will="" provide="" information="" on="" this="" method="" to="" fda.="" in="" the="" interim,="" the="" analytical="" method="" is="" available="" to="" anyone="" who="" is="" interested="" in="" pesticide="" residue="" enforcement="" from:="" by="" mail,="" calvin="" furlow,="" public="" information="" and="" records="" integrity="" branch,="" information="" resources="" and="" services="" division="" (7502c),="" office="" of="" pesticide="" programs,="" environmental="" protection="" agency,="" 401="" m="" st.,="" sw.,="" washington,="" dc="" 20460.="" office="" location="" and="" telephone="" number:="" crystal="" mall="" #2,="" rm.="" 1128,="" 1921="" jefferson="" davis="" hwy.,="" arlington,="" va="" 22202,="" 703-305-5805.="" c.="" magnitude="" of="" residues="" a="" report="" entitled="" ``reanalysis="" of="" chronic="" and="" acute="" exposure="" and="" risk="" for="" lambda-cyhalothrin="" residues''="" contains="" revisions="" to="" the="" originally="" submitted="" report:="" ``chronic="" and="" acute="" dietary="" exposure="" analyses="" and="" risk="" assessment="" for="" lambda-cyhalothrin="" residues="" in="" food.''="" the="" report="" dated="" october="" 10,="" 1997="" contains="" a="" list="" of="" all="" residue="" values="" used="" in="" the="" chronic="" and="" acute="" dietary="" exposure="" analyses="" (including="" drinking="" water).="" the="" residue="" values="" have="" been="" verified="" by="" epa="" and="" are="" appropriate.="" d.="" international="" residue="" limits="" no="" codex="" mrls="" for="" residues="" of="" lambda-cyhalothrin="" have="" been="" established.="" canadian="" mrls="" have="" been="" established="" for="" residues="" of="" lambda-cyhalothrin.="" mexico="" has="" established="" tolerances="" for="" residues="" of="" lambda-cyhalothrin="" on="" cottonseed="" (0.05="" ppm)="" which="" is="" in="" harmony="" with="" the="" u.s.="" tolerance.="" mexico="" has="" established="" tolerances="" which="" are="" below="" their="" u.s.="" counterparts="" for="" corn="" grain="" (0.01="" vs.="" 0.05="" ppm)="" and="" sorghum="" grain="" (0.1="" vs.="" 0.2="" ppm).="" as="" indicated="" above="" there="" are="" differences="" between="" the="" section="" 408="" tolerances="" and="" the="" codex="" mrl="" values="" for="" specific="" commodities.="" these="" differences="" could="" be="" caused="" by="" differences="" in="" methods="" used="" to="" establish="" tolerances,="" calculate="" animal="" feed="" dietary="" exposure,="" and="" as="" a="" result="" of="" different="" agricultural="" practices.="" epa="" will="" specifically="" address="" these="" differences="" when="" the="" pesticides="" are="" reregistered="" and="" the="" tolerances="" made="" permanent.="" iv.="" conclusion="" therefore,="" tolerances="" are="" established="" for="" lambda-cyhalothrin="" and="" its="" epimer="" in="" or="" on="" broccoli="" at="" 0.4="" ppm;="" cabbage="" at="" 0.4="" ppm;="" cattle,="" fat="" at="" 3.0="" ppm;="" cattle,="" meat="" at="" 0.2="" ppm;="" cattle,="" meat="" and="" meat="" by-="" products="" (mbyp)="" at="" 0.2="" ppm;="" corn,="" grain="" (field="" and="" pop)="" at="" 0.05="" ppm;="" corn,="" fodder="" at="" 1.0="" ppm;="" corn,="" forage="" at="" 6.0="" ppm;="" corn,="" sweet="" (k+kwhr)="" at="" 0.05="" ppm;="" cottonseed="" at="" 0.05="" ppm;="" dry="" bulb="" onion="" at="" 0.1="" ppm;="" eggs="" at="" 0.01="" ppm;="" garlic="" at="" 0.1="" ppm;="" goats,="" fat="" at="" 3.0="" ppm;="" goats,="" meat="" at="" 0.2="" ppm;="" goats,="" mbyp="" at="" 0.2="" ppm,="" hogs,="" fat="" at="" 3.0="" ppm;="" hogs,="" meat="" at="" 0.2="" ppm;="" hogs,="" mbyp="" at="" 0.2="" ppm;="" horses,="" fat="" at="" 3.0="" ppm;="" horses,="" meat="" at="" 0.2="" ppm;="" horses,="" mbyp="" at="" 0.2="" ppm;="" lettuce,="" head="" at="" 2.0="" ppm;="" milk,="" fat="" (reflecting="" 0.2="" ppm="" in="" whole="" milk)="" at="" 5.0="" ppm;="" peanuts="" at="" 0.05="" ppm;="" peanuts,="" hulls="" at="" 0.05="" ppm;="" poultry,="" fat="" at="" 0.01="" ppm;="" poultry,="" meat="" at="" 0.01="" ppm;="" poultry,="" mbyp="" at="" 0.01="" ppm;="" rice,="" grain="" at="" 1.0="" ppm;="" rice,="" hulls="" at="" 5.0="" ppm;="" rice,="" straw="" at="" 1.8="" ppm;="" sheep,="" fat="" at="" 3.0="" ppm;="" sheep,="" meat="" at="" 0.2="" ppm;="" sheep,="" mbyp="" at="" 0.2="" ppm;="" soybeans="" at="" 0.01="" ppm;="" sorghum,="" grain="" at="" 0.02="" ppm;="" sorghum,="" grain="" dust="" at="" 1.5="" ppm;="" sunflower,="" seeds="" at="" 0.2="" ppm;="" sunflower,="" forage="" at="" 0.2="" ppm;="" tomatoes="" at="" 0.1="" ppm;="" wheat,="" grain="" at="" 0.05="" ppm;="" wheat,="" forage="" at="" 2.0="" ppm;="" wheat,="" hay="" at="" 2.0="" ppm;="" wheat,="" straw="" at="" 2.0="" ppm;="" wheat,="" grain="" dust="" at="" 2.0="" ppm;="" corn,="" grain="" flour="" at="" 0.15="" ppm;="" sunflower,="" oil="" at="" 0.30="" ppm;="" sunflower,="" hulls="" at="" 0.50="" ppm;="" tomato="" pomace="" (dry="" or="" wet)="" at="" 6.0="" ppm;="" and="" wheat,="" bran="" at="" 0.2="" ppm.="" [[page="" 63009]]="" in="" addition="" to="" the="" tolerance="" being="" amended,="" since="" for="" purposes="" of="" establishing="" tolerances="" fqpa="" has="" eliminated="" all="" distinctions="" between="" raw="" and="" processed="" food,="" epa="" is="" combining="" the="" tolerances="" that="" now="" appear="" in="" secs.="" 185.3765="" and="" 186.3765="" with="" the="" tolerances="" in="" sec.="" 180.438="" and="" is="" removing="" secs.="" 185.3765="" and="" 186.3765.="" v.="" objections="" and="" hearing="" requests="" the="" new="" ffdca="" section="" 408(g)="" provides="" essentially="" the="" same="" process="" for="" persons="" to="" ``object''="" to="" a="" tolerance="" regulation="" issued="" by="" epa="" under="" new="" section="" 408(e)="" and="" (l)(6)="" as="" was="" provided="" in="" the="" old="" section="" 408="" and="" in="" section="" 409.="" however,="" the="" period="" for="" filing="" objections="" is="" 60="" days,="" rather="" than="" 30="" days.="" epa="" currently="" has="" procedural="" regulations="" which="" govern="" the="" submission="" of="" objections="" and="" hearing="" requests.="" these="" regulations="" will="" require="" some="" modification="" to="" reflect="" the="" new="" law.="" however,="" until="" those="" modifications="" can="" be="" made,="" epa="" will="" continue="" to="" use="" those="" procedural="" regulations="" with="" appropriate="" adjustments="" to="" reflect="" the="" new="" law.="" any="" person="" may,="" by="" january="" 26,="" 1998,="" file="" written="" objections="" to="" any="" aspect="" of="" this="" regulation="" and="" may="" also="" request="" a="" hearing="" on="" those="" objections.="" objections="" and="" hearing="" requests="" must="" be="" filed="" with="" the="" hearing="" clerk,="" at="" the="" address="" given="" above="" (40="" cfr="" 178.20).="" a="" copy="" of="" the="" objections="" and/or="" hearing="" requests="" filed="" with="" the="" hearing="" clerk="" should="" be="" submitted="" to="" the="" opp="" docket="" for="" this="" rulemaking.="" the="" objections="" submitted="" must="" specify="" the="" provisions="" of="" the="" regulation="" deemed="" objectionable="" and="" the="" grounds="" for="" the="" objections="" (40="" cfr="" 178.25).="" each="" objection="" must="" be="" accompanied="" by="" the="" fee="" prescribed="" by="" 40="" cfr="" 180.33(i).="" if="" a="" hearing="" is="" requested,="" the="" objections="" must="" include="" a="" statement="" of="" the="" factual="" issues="" on="" which="" a="" hearing="" is="" requested,="" the="" requestor's="" contentions="" on="" such="" issues,="" and="" a="" summary="" of="" any="" evidence="" relied="" upon="" by="" the="" requestor="" (40="" cfr="" 178.27).="" a="" request="" for="" a="" hearing="" will="" be="" granted="" if="" the="" administrator="" determines="" that="" the="" material="" submitted="" shows="" the="" following:="" there="" is="" genuine="" and="" substantial="" issue="" of="" fact;="" there="" is="" a="" reasonable="" possibility="" that="" available="" evidence="" identified="" by="" the="" requestor="" would,="" if="" established,="" resolve="" one="" or="" more="" of="" such="" issues="" in="" favor="" of="" the="" requestor,="" taking="" into="" account="" uncontested="" claims="" or="" facts="" to="" the="" contrary;="" and="" resolution="" of="" the="" factual="" issues="" in="" the="" manner="" sought="" by="" the="" requestor="" would="" be="" adequate="" to="" justify="" the="" action="" requested="" (40="" cfr="" 178.32).="" information="" submitted="" in="" connection="" with="" an="" objection="" or="" hearing="" request="" may="" be="" claimed="" confidential="" by="" marking="" any="" part="" or="" all="" of="" that="" information="" as="" confidential="" business="" information="" (cbi).="" information="" so="" marked="" will="" not="" be="" disclosed="" except="" in="" accordance="" with="" procedures="" set="" forth="" in="" 40="" cfr="" part="" 2.="" a="" copy="" of="" the="" information="" that="" does="" not="" contain="" cbi="" must="" be="" submitted="" for="" inclusion="" in="" the="" public="" record.="" information="" not="" marked="" confidential="" may="" be="" disclosed="" publicly="" by="" epa="" without="" prior="" notice.="" vi.="" public="" record="" and="" electronic="" submissions="" epa="" has="" established="" a="" record="" for="" this="" rulemaking="" under="" docket="" control="" number="" [opp-300581]="" (including="" any="" comments="" and="" data="" submitted="" electronically).="" a="" public="" version="" of="" this="" record,="" including="" printed,="" paper="" versions="" of="" electronic="" comments,="" which="" does="" not="" include="" any="" information="" claimed="" as="" cbi,="" is="" available="" for="" inspection="" from="" 8:30="" a.m.="" to="" 4="" p.m.,="" monday="" through="" friday,="" excluding="" legal="" holidays.="" the="" public="" record="" is="" located="" in="" room="" 1132="" of="" the="" public="" information="" and="" records="" integrity="" branch,="" information="" resources="" and="" services="" division="" (7502c),="" office="" of="" pesticide="" programs,="" environmental="" protection="" agency,="" crystal="" mall="" #2,="" 1921="" jefferson="" davis="" highway,="" arlington,="" va.="" electronic="" comments="" may="" be="" sent="" directly="" to="" epa="" at:="">opp-docket@epamail.epa.gov.
    
        Electronic comments must be submitted as an ASCII file avoiding the 
    use of special characters and any form of encryption.
        The official record for this rulemaking, as well as the public 
    version, as described above will be kept in paper form. Accordingly, 
    EPA will transfer any copies of objections and hearing requests 
    received electronically into printed, paper form as they are received 
    and will place the paper copies in the official rulemaking record which 
    will also include all comments submitted directly in writing. The 
    official rulemaking record is the paper record maintained at the 
    Virginia address in ``ADDRESSES'' at the beginning of this document.
    
    VII. Regulatory Assessment Requirements
    
        This final rule establishes tolerances under FFDCA section 408(d) 
    in response to a petition submitted to the Agency. The Office of 
    Management and Budget (OMB) has exempted these types of actions from 
    review under Executive Order 12866, entitled Regulatory Planning and 
    Review (58 FR 51735, October 4, 1993). This final rule does not contain 
    any information collections subject to OMB approval under the Paperwork 
    Reduction Act (PRA), 44 U.S.C. 3501 et seq., or impose any enforceable 
    duty or contain any unfunded mandate as described under Title II of the 
    Unfunded Mandates Reform Act of 1995 (UMRA) (Pub. L. 104-4). Nor does 
    it require any prior consultation as specified by Executive Order 
    12875, entitled Enhancing the Intergovernmental Partnership (58 FR 
    58093, October 28, 1993), or special considerations as required by 
    Executive Order 12898, entitled Federal Actions to Address 
    Environmental Justice in Minority Populations and Low-Income 
    Populations (59 FR 7629, February 16, 1994), or require OMB review in 
    accordance with Executive Order 13045, entitled Protection of Children 
    from Environmental Health Risks and Safety Risks (62 FR 19885, April 
    23, 1997).
        In addition, since these tolerances are established on the basis of 
    a petition under FFDCA section 408(d), such as the tolerance in this 
    final rule, do not require the issuance of a proposed rule, the 
    requirements of the Regulatory Flexibility Act (RFA) (5 U.S.C. 601 et 
    seq.) do not apply. Nevertheless, the Agency has previously assessed 
    whether establishing tolerances, exemptions from tolerances, raising 
    tolerance levels or expanding exemptions might adversely impact small 
    entities and concluded, as a generic matter, that there is no adverse 
    economic impact. The factual basis for the Agency's generic 
    certification for tolerance actions published on May 4, 1981 (46 FR 
    24950) and was provided to the Chief Counsel for Advocacy of the Small 
    Business Administration.
    
    VIII. Submission to Congress and the General Accounting Office
    
        Under 5 U.S.C. 801(a)(1)(A), as added by the Small Business 
    Regulatory Enforcement Fairness Act of 1996, the Agency has submitted a 
    report containing this rule and other required information to the U.S. 
    Senate, the U.S. House of Representatives, and the Comptroller General 
    of the General Accounting Office prior to publication of this rule in 
    today's Federal Register. This is not a ``major rule'' as defined by 5 
    U.S.C. 804(2).
    
    List of Subjects
    
    40 CFR Part 180
    
        Environmental protection, Administrative practice and procedure, 
    Agricultural commodities, Pesticides and pests, Reporting and 
    recordkeeping requirements.
    
    [[Page 63010]]
    
    40 CFR Part 185
    
        Environmental protection, Food additives, Pesticides and pests.
    
    40 CFR Part 186
    
        Environmental protection, Feed additives, Pesticides and pests.
    
        Dated: November 14, 1997.
    James Jones,
    Acting Director, Registration Division Office of Pesticide Programs.
        Therefore, 40 CFR chapter I is amended as follows:
    
    PART 180--[AMENDED]
    
        1. In part 180:
        a. The authority citation for part 180 continues to read as 
    follows:
    
        Authority: 21 U.S.C. 346a and 371.
        b. Section 180.438 is amended by revising paragraph (a) to read as 
    follows:
    
    
    Sec. 180.438   Lambda-cyhalothrin; tolerances for residues.
    
        (a) General. (1) Tolerances are established for the combined 
    residues of the pyrethroid lambda-cyhalothrin, 1:1 mixture of (S)-
    -cyano-3-phenoxybenzyl-(Z)-(1R,3R)-3-(2-chloro-3,3,3- 
    trifluoroprop-1-enyl)-2,2- dimethylcyclopropanecarboxylate and (R)-
    -cyano-3-phenoxybenzyl-(Z)-(1S,3S)-3-(2-chloro-3,3,3- 
    trifluoroprop-1-enyl)-2,2- dimethylcyclopropanecarboxylate and its 
    epimer expressed as epimer of lambda-cyhalothrin, a 1:1 mixture of (S)-
    -cyano-3-phenoxybenzyl-(Z)-(1S,3S)-3-(2-chloro-3,3,3-
    trifluoroprop-1-enyl)-2,2- dimethylcyclopropanecarboxylate and (R)-
    -cyano-3- phenoxybenzyl-(Z)-(1R,3R)-3-(2-chloro-3,3,3- 
    trifluoroprop-1-enyl)-2,2- dimethylcyclopropanecarboxylate, on plants 
    and livestocks, as indicated in the following table.
    
    ------------------------------------------------------------------------
                     Commodity                        Parts per million     
    ------------------------------------------------------------------------
    Broccoli..................................  0.4                         
    Cabbage...................................  0.4                         
    Cattle, fat...............................  3.0                         
    Cattle, meat..............................  0.2                         
    Cattle, mbyp..............................  0.2                         
    Corn, grain (field and pop)...............  0.05                        
    Corn, fodder..............................  1.0                         
    Corn, forage..............................  6.0                         
    Corn, grain flour.........................  0.15                        
    Corn, sweet (K+kwhr)......................  0.05                        
    Cottonseed................................  0.05                        
    Dry bulb onion............................  0.1                         
    Eggs......................................  0.01                        
    Garlic....................................  0.1                         
    Goats, fat................................  3.0                         
    Goats, meat...............................  0.2                         
    Goats, mbyp...............................  0.2                         
    Hogs, fat.................................  3.0                         
    Hogs, meat................................  0.2                         
    Hogs, mbyp................................  0.2                         
    Horses, fat...............................  3.0                         
    Horses, meat..............................  0.2                         
    Horses, mbyp..............................  0.2                         
    Lettuce, head.............................  2.0                         
    Milk, fat (reflecting 0.2 ppm in whole      5.0                         
     milk).                                                                 
    Peanuts...................................  0.05                        
    Peanuts, hulls............................  0.05                        
    Poultry, fat..............................  0.01                        
    Poultry, meat.............................  0.01                        
    Poultry, mbyp.............................  0.01                        
    Rice, grain...............................  1.0                         
    Rice, hulls...............................  5.0                         
    Rice, straw...............................  1.8                         
    Sheep, fat................................  3.0                         
    Sheep, meat...............................  0.2                         
    Sheep, mbyp...............................  0.2                         
    Soybeans..................................  0.01                        
    Sorghum, grain............................  0.2                         
    Sorghum, grain dust.......................  1.5                         
    Sunflower, forage.........................  0.2                         
    Sunflower, hulls..........................  0.50                        
    Sunflower, oil............................  0.30                        
    Sunflowers, seeds.........................  0.2                         
    Tomatoes..................................  0.1                         
    Tomato pomace (dry or wet)................  6.0                         
    Wheat, grain..............................  0.05                        
    Wheat, forage.............................  2.0                         
    Wheat, hay................................  2.0                         
    Wheat, straw..............................  2.0                         
    Wheat, grain dust.........................  2.0                         
    Wheat, bran...............................  0.2                         
    ------------------------------------------------------------------------
    
        (2) A food additive tolerance of 0.01 part per million is 
    established for residues of the insecticide 
    [1(S*),3(Z)]-()-cyano(3-
    phenoxyphenyl)methyl 3-(2-chloro-3,3,3-trifluoro-1-propenyl)-2,2-
    dimethylcyclopropanecarboxylate (lambdacyhalothrin) as follows:
        (i) In or on all food items (other than those already covered by a 
    higher tolerance as a result of use on growing crops) in food-handling 
    establishments where food products are held, processed, or prepared.
        (ii) Application shall be limited solely to spot and/or crack and 
    crevice treatment with a spray solution maximum of a 0.06-percent 
    active ingredient by weight. Food must be removed or covered during 
    treatment. Spray should not be applied directly to surfaces or utensils 
    that may come into contact with food. Food-contact surfaces and 
    equipment should be thoroughly cleaned with an effective cleaning 
    compound and rinsed with potable water before using.
        (iii) For spot treatment, a coarse low-pressure spray shall be 
    used. Limit individual spot treatments to an area no larger than 20 
    percent of the surface area. Any individual spot treatment shall not 
    exceed 2 square feet.
        (iv) For crack and crevice treatment, equipment capable of 
    delivering a pin-stream of spray directly into the cracks and crevices 
    shall be used.
        (v) To assure safe use of the additive, its label and labeling 
    shall conform to that registered with the U.S. Environmental Protection 
    Agency, and it shall be used in accordance with such label and 
    labeling.
        (3) A food additive tolerance is established for residues of the 
    insecticide [1 (S*),3(Z)]-()-cyano-(3-
    phenoxylphenyl)methyl 3-(2-chloro-3,3,3-trifluoro-1-propenyl)-2,2-
    dimethylcyclopropanecarboxylate as follows:
    
    ------------------------------------------------------------------------
                                                                  Parts per 
                             Commodity                             million  
    ------------------------------------------------------------------------
    Hops, dried................................................         10.0
    ------------------------------------------------------------------------
    
    *       *       *       *       *
    
    PART 185--[AMENDED]
    
        2. In part 185:
        a. The authority citation for part 185 continues to read as 
    follows:
    
        Authority: 21 U.S.C. 348.
    
    
    Sec. 185.3765  [Removed]
    
        b. Section 185.3765 is removed.
    
    PART 186--[AMENDED]
    
        3. In part 186:
        a. The authority citation for part 186 continues to read as 
    follows:
    
        Authority: 21 U.S.C. 346a and 371.
    
    
    Sec. 186.3765  [Removed]
    
        b. Section 186.3765 is removed.
    
    [FR Doc. 97-30959 Filed 11-25-97; 8:45 am]
    BILLING CODE 6560-50-F
    
    
    

Document Information

Effective Date:
11/26/1997
Published:
11/26/1997
Department:
Environmental Protection Agency
Entry Type:
Rule
Action:
Final rule.
Document Number:
97-30959
Dates:
This regulation is effective November 26, 1997. Objections and requests for hearings must be received by EPA on or before January 28, 1998.
Pages:
63002-63010 (9 pages)
Docket Numbers:
OPP-300581, FRL-5755-5
RINs:
2070-AB78
PDF File:
97-30959.pdf
CFR: (3)
40 CFR 180.438
40 CFR 185.3765
40 CFR 186.3765