95-24004. Fenpropathrin; Pesticide Tolerance  

  • [Federal Register Volume 60, Number 187 (Wednesday, September 27, 1995)]
    [Rules and Regulations]
    [Pages 49793-49795]
    From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
    [FR Doc No: 95-24004]
    
    
    
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    ENVIRONMENTAL PROTECTION AGENCY
    40 CFR Part 180
    
    [PP 3F4186/R2174; FRL-4979-1]
    RIN 2070-AB78
    
    
    Fenpropathrin; Pesticide Tolerance
    
    AGENCY: Environmental Protection Agency (EPA).
    
    ACTION: Final rule.
    
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    SUMMARY: This rule establishes time-limited tolerances with an 
    expiration date of November 15, 1997, for residues of the pyrethroid 
    fenpropathrin in or on the raw agricultural commodities (RACs) 
    strawberries and tomatoes. Valent U.S.A. submitted petitions under the 
    Federal Food, Drug and Cosmetic Act (FFDCA) that requested a regulation 
    to establish these maximum permissible levels for residues of the 
    insecticide.
    
    EFFECTIVE DATE: This regulation becomes effective September 27, 1995.
    
    ADDRESSES: Written objections and hearing requests, identified by the 
    document control number [PP 3F4186/R2174], may be submitted to: Hearing 
    Clerk (1900), Environmental Protection Agency, Rm. M3708, 401 M St., 
    SW., Washington, DC 20460. A copy of any objections and hearing 
    requests filed with the Hearing Clerk should be identified by the 
    document control number and submitted to: Public Response and Program 
    Resources Branch, Field Operations Division (7506C), Office of 
    Pesticide Programs, Environmental Protection Agency, 401 M St., SW., 
    Washington, DC 20460. In person, bring copy of objections and hearing 
    requests to Rm. 1132, CM #2, 1921 Jefferson Davis Hwy., Arlington, VA 
    22202. Fees accompanying objections 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 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 in 5.1 
    file format or ASCII file format. All copies of objections and hearing 
    requests in electronic form must be identified by the docket number [PP 
    3F4186/R2174]. 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. Additional information on electronic submissions can be 
    found below in this document.
    FOR FURTHER INFORMATION CONTACT: By mail: George T. LaRocca, Product 
    Manager (PM) 13, Registration Division (7505C), Office of Pesticide 
    Programs, Environmental Protection Agency, 401 M St., SW., Washington, 
    DC 20460. Office location and telephone number: Second Floor, Crystal 
    Mall #2, 1921 Jefferson Davis Highway, Arlington, VA 22202, (703)-305-
    6100; e-mail: larocca.george@epamail.epa.gov.
    
    SUPPLEMENTARY INFORMATION: EPA issued notices, published in the Federal 
    Register of October 21, 1993 (58 FR 54354), which announced that Valent 
    U.S.A. Corp., 1333 N. California Blvd., Suite 600, Walnut Creek, CA 
    94596, had submitted pesticide petition (PP) 3F4186 and food/feed 
    additive petition (FAP) 3H5661 to EPA requesting that the 
    Administrator, pursuant to sections 408(d) and 409(b) of the Federal 
    Food, Drug, and Cosmetic Act (FFDCA), 21 U.S.C. 346a(d) and 348(b), 
    establish tolerances for residues of the insecticide fenpropathrin 
    (alpha-cyano-3-phenoxybenzyl 2,2,3,3-
    tetramethylcyclopropanecarboxylate) in or on the raw agricultural 
    commodities (RACs) strawberries at 2 parts per million (PPM); tomatoes 
    (fresh market, Florida only) at 0.5 ppm; and tomato cannery waste at 5 
    ppm. EPA issued a revised notice, published in the Federal Register of 
    November 2, 1994 (59 FR 54911), in which Valent U.S.A. proposed to 
    amend PP 3F4186 by increasing the tolerances for fenpropathrin in or on 
    the RAC tomatoes from 0.5 to 0.6 ppm and removing the fresh marketing 
    regional restrictions for tomatoes; establish tolerances for 
    fenpropathrin in or on strawberries (caps removed) at 2.0 ppm; meat and 
    meat byproducts of cattle, goats, hogs, horses, and sheep at 0.1 ppm; 
    fat of cattle, goats, hogs, horses, and sheep at 1.0 ppm; milk fat 
    (reflecting 0.11 ppm in whole milk) at 2.75 ppm; poultry meat, fat, and 
    meat byproducts and eggs at 0.02 ppm; and amending the FAP 3H5661 by 
    replacing the proposed tomato cannery waste tolerance with proposals 
    for tolerances in or on tomato pomaces (wet) at 6.00 ppm and tomato 
    pomaces (dry) at 3.00 ppm.
        In a letter dated August 30, 1995, Valent U.S.A. requested 
    withdrawal of the feed additive petition (3H5661) in or on tomato 
    pomaces and deletion of the proposed tolerances in meat, milk, poultry, 
    and eggs. Valent U.S.A.'s withdrawal and deletion of certain tolerances 
    were submitted in response to EPA's latest revision (unpublished) to 
    Table II of the Pesticide Assessment Guidelines, Subdivision O (Residue 
    Chemistry) Raw Agricultural and Processed Commodities and Livestock 
    Feeds Derived from Field Crops. With respect to tomatoes, EPA concluded 
    that tomato pomaces (wet and dry) are no longer considered significant 
    animal feedstuffs. Although the latest revisions to the Livestock Feed 
    Table for Subdivision O of the Pesticide Assessment Guidelines have not 
    yet been published, pending petitions will continue to be processed 
    based upon previous regulations, except they will be given the benefit 
    of any appropriate revised or reduced residue data requirements if 
    needed.
        No comments were received in response to the notices of filing.
        The scientific data submitted in the petitions and other relevant 
    material have been evaluated. The toxicological and metabolism data and 
    analytical methods for enforcement purposes considered in support of 
    these tolerances are discussed in detail in related documents published 
    in the Federal Register of April 14, 1993 (58 FR 19357).
        A dietary exposure/risk assessment was performed for fenpropathrin 
    using a Reference Dose (RfD) of 0.025 mg/kg/day. The RfD is based on a 
    no-observable- effect level (NOEL) of 2.5 mg/kg/body weight/day (100 
    ppm) and a uncertainty factor of 100 from a 1-year dog-feeding study 
    that demonstrated tremors in test animals at the lowest effect level. 
    The current estimated dietary exposure for the overall U.S. population 
    and nonnursing infants (less than 1 year old), the subgroup population 
    exposed to the highest risk, is 0.4% and 0.5% of the RfD, respectively. 
    The current action will increase exposure to 4.1% and 3%, respectively. 
    Generally speaking, the Agency has no cause for concern if total 
    residue contribution for published and proposed tolerances is less than 
    the RfD.
        The metabolism of the chemical in plants and livestock is 
    adequately understood for this use. Any secondary residues occurring in 
    meat, fat, meat by products of cattle, goats, hogs, horses, poultry, 
    sheep and eggs will be covered by the existing tolerances. An adequate 
    
    [[Page 49794]]
    analytical method (gas liquid chromatography with an electron capture 
    detector) is available for enforcement purposes. The enforcement 
    methodology has been submitted to the Food and Drug Administration and 
    published in the Pesticide Analytical Manual Vol. II (PAM II).
        The Agency issued a conditional registration for fenpropathrin for 
    use on cotton with an expiration date of November 15, 1993 (see the 
    Federal Register of April 14, 1993 (58 FR 19357)). The conditional 
    registration was subsequently amended and extended to November 15, 1996 
    (see the Federal Register dated February 22, 1995 (60 FR 9783)). The 
    registrations were amended and extended to allow time for submission 
    and evaluation of additional environmental effects data. In order to 
    evaluate the effects of the pyrethroids on fish and aquatic organisms 
    and its fate in the environment, additional data were required to be 
    collected and submitted during the period of conditional registration. 
    Such requirements included a sediment bioavailability and toxicity 
    study and a small-plot runoff study that must be submitted to the 
    Agency by July 1, 1996. Due to the conditional status of the 
    registration, tolerances have been established for fenpropathrin on a 
    temporary basis, (until November 15, 1997) on cottonseed, meat, fat and 
    meat-byproducts of hogs, horses, cattle, goats, sheep, poultry, eggs, 
    and milk to cover residues expected to be present from use during the 
    period of conditional registration. To be consistent with the 
    conditional registration status of fenpropathrin on cotton the Agency 
    is establishing these tolerances with an expiration date of November 
    15, 1997.
        Residues remaining in or on the above commodities after expiration 
    of these tolerances will not be considered actionable if the pesticide 
    is legally applied during the term of and in accordance with provisions 
    of the conditional registration.
        There are currently no actions pending against the continued 
    registration of this chemical. The pesticide is considered useful for 
    the purposes which it is sought and capable of achieving the intended 
    physical or technical effect. Based on the information and data 
    considered, the Agency has determined that the tolerances established 
    by amending 40 CFR part 180 will protect the public health. Therefore, 
    the tolerances are established as set forth below.
        Any person adversely affected by this regulation may, within 30 
    days after publication of this document in the Federal Register, file 
    written objections to the 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 issue(s) on which a hearing is requested, the 
    requestor's contentions on such issues, and a summary of any evidence 
    relied upon by the objector (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 issue(s) in the manner sought by the requestor would be 
    adequate to justify the action requested (40 CFR 178.32).
         A record has been established for this rulemaking under docket 
    number [PP 3F4186/R2174] (including objections and hearing requests 
    submitted electronically as described below). 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 a.m. to 4:30 p.m., Monday through Friday, excluding 
    legal holidays. The public record is located in Room 1132 of the Public 
    Response and Program Resources Branch, Field Operations Division 
    (7506C), Office of Pesticide Programs, Environmental Protection Agency, 
    Crystal Mall #2, 1921 Jefferson Davis Highway, Arlington, VA.
        Written objections and hearing requests, identified by the document 
    control number [PP 3F4186/R2174], may be submitted to the Hearing Clerk 
    (1900), Environmental Protection Agency, Rm. 3708, 401 M St., SW., 
    Washington, DC 20460.
        A copy of electronic objections and hearing requests filed with the 
    Hearing Clerk can be sent directly to EPA at:
        opp-Docket@epamail.epa.gov
    
    
        A copy of electronic objections and hearing requests filed with the 
    Hearing Clerk 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 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 objections and hearing requests submitted directly in 
    writing. The official rulemaking record is the paper record maintained 
    at the address in ``ADDRESSES'' at the beginning of this document.
        Under Executive Order 12866 (58 FR 51735, October 4, 1993), the 
    Agency must determine whether the regulatory action is ``significant'' 
    and therefore subject to all the requirements of the Executive Order 
    (i.e., Regulatory Impact Analysis, review by the Office of Management 
    and Budget (OMB)). Under section 3(f), the order defines 
    ``significant'' as those actions likely to lead to a rule (1) having an 
    annual effect on the economy of $100 million or more, or adversely and 
    materially affecting a sector of the economy, productivity, 
    competition, jobs, the environment, public health or safety, or State, 
    local or tribal governments or communities (also known as 
    ``economically significant''); (2) creating serious inconsistency or 
    otherwise interfering with an action taken or planned by another 
    agency; (3) materially altering the budgetary impacts of entitlement, 
    grants, user fees, or loan programs; or (4) raising novel legal or 
    policy issues arising out of legal mandates, the President's 
    priorities, or the principles set forth in this Executive Order.
        Pursuant to the terms of this Executive Order, EPA has determined 
    that this rule is not ``significant'' and is therefore not subject to 
    OMB review.
        Pursuant to the requirements of the Regulatory Flexibility Act 
    (Pub. L. 96-354, 94 Stat. 1164, 5 U.S.C. 601-612), the Administrator 
    has determined that regulations establishing new tolerances or raising 
    tolerance levels or establishing exemptions from tolerance requirements 
    do not have a significant economic impact on a substantial number of 
    small entities. A certification statement to this effect was published 
    in the Federal Register of May 4, 1981 (46 FR 24950).
    
    List of Subjects in 40 CFR Part 180
    
        Environmental Protection, Administrative practice and procedure, 
    Agricultural commodities, Pesticides 
    
    [[Page 49795]]
    and pests, Reporting and recordkeeping requirements.
    
        Dated: September 15, 1995.
    
    Peter Caulkins,
    Acting Director, Registration Division, Office of Pesticide Programs.
    
    PART 180--[AMENDED]
    
        Therefore, 40 CFR part 180 is amended as follows:
        1. The authority citation for part 180 continues to read as 
    follows:
    
        Authority: 21 U.S.C. 346a and 371.
    
        2. By amending Sec. 180.466 in the table therein by adding and 
    alphabetically inserting entries for the commodities tomatoes and 
    strawberries, to read as follows:
    
    
    Sec. 180.466   Fenpropathrin; tolerances for residues.
    
    * * * * *
    
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                                                     Parts per    Expiration
                       Commodity                      million        date   
    ------------------------------------------------------------------------
                                                                            
                      *        *        *        *        *                 
    Strawberries..................................          2.0          Do.
    Tomatoes......................................          0.6          Do.
                                                                            
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    [FR Doc. 95-24004 Filed 9-26-95; 8:45 am]
    BILLING CODE 6560-50-F
    
    

Document Information

Effective Date:
9/27/1995
Published:
09/27/1995
Department:
Environmental Protection Agency
Entry Type:
Rule
Action:
Final rule.
Document Number:
95-24004
Dates:
This regulation becomes effective September 27, 1995.
Pages:
49793-49795 (3 pages)
Docket Numbers:
PP 3F4186/R2174, FRL-4979-1
RINs:
2070-AB78
PDF File:
95-24004.pdf
CFR: (1)
40 CFR 180.466