96-19305. Direct Food Substances Affirmed as Generally Recognized as Safe; Listing of Color Additives Exempt From Certification; Ferrous Lactate  

  • [Federal Register Volume 61, Number 150 (Friday, August 2, 1996)]
    [Rules and Regulations]
    [Pages 40317-40320]
    From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
    [FR Doc No: 96-19305]
    
    
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    DEPARTMENT OF HEALTH AND HUMAN SERVICES
    
    Food and Drug Administration
    
    21 CFR Parts 73 and 184
    
    [Docket No. 93G-0017]
    
    
    Direct Food Substances Affirmed as Generally Recognized as Safe; 
    Listing of Color Additives Exempt From Certification; Ferrous Lactate
    
    AGENCY: Food and Drug Administration, HHS.
    
    ACTION: Final rule.
    
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    SUMMARY: The Food and Drug Administration (FDA) is amending its 
    regulations to affirm that ferrous lactate is generally recognized as 
    safe (GRAS) as a color fixative on ripe olives. The agency is adding 
    this use of ferrous lactate as a color fixative on ripe olives to the 
    other uses for ferrous lactate. The agency is also amending this 
    regulation to permit additional methods of synthesis for ferrous 
    lactate. This action is in response to a petition filed by Purac 
    America, Inc. The agency, on its own initiative, is also amending its 
    color additive regulations to provide for the safe use of ferrous 
    lactate for the coloring of ripe olives.
    
    DATES: The amendments to Sec. 184.1311 (21 CFR 184.1311) will be 
    effective on August 2, 1996. New Sec. 73.165 will be effective on 
    September 4, 1996, except as to any provisions that may be stayed by 
    the filing of proper objections; written objections by September 3, 
    1996. The Director of the Office of the Federal Register approves the 
    incorporations by reference in accordance with 5 U.S.C. 552(a) and 1 
    CFR part 51 of certain publications listed in Sec. 184.1311(b), 
    effective August 2, 1996; and in new Sec. 73.165(b) effective September 
    4, 1996.
    
    ADDRESSES: Submit written objections to new Sec. 73.165 to the Dockets 
    Management Branch (HFA-305), Food and Drug Administration, 12420 
    Parklawn Dr., rm. 1-23, Rockville, MD 20857.
    
    FOR FURTHER INFORMATION CONTACT: Robert L. Martin, Center for Food 
    Safety and Applied Nutrition (HFS-217), Food and Drug Administration, 
    200 C St. SW., Washington, DC 20204, 202-418-3074.
    
    SUPPLEMENTARY INFORMATION:
    
    I. Background
    
        In accordance with the procedures described in 21 CFR 170.35, Purac 
    America, Inc., c/o 700 13th St. NW., suite 1200, Washington, DC 20005, 
    submitted a petition (GRASP 3G0396) requesting that the regulations in 
    Sec. 184.1311 be amended to affirm that ferrous lactate is GRAS as a 
    color fixative in black olives.
        FDA published a notice of filing of this petition in the Federal 
    Register of December 27, 1993 (58 FR 68437), and gave interested 
    parties an opportunity to submit comments to the Dockets Management 
    Branch (HFA-305), Food and Drug Administration, 12420 Parklawn Dr., rm. 
    1-23, Rockville, MD 20857. Also, in this notice, FDA announced that, on 
    its own initiative, the agency would amend the color additive 
    regulations to provide for the safe use of ferrous lactate as a color 
    additive for the coloring of ripe olives. No comments were received in 
    response to this notice of filing.
        Since the filing of this petition, the agency has come to recognize 
    that ferrous lactate is being used as a color fixative in ripe, rather 
    than black, olives. The Agricultural Marketing Service of the U. S. 
    Department of Agriculture defines ``ripe type'' olives as ``* * * those 
    which have been treated and oxidized in processing to produce a typical 
    dark brown to black color'' (7 CFR 52.3752(a)). Also, in 21 CFR 73.160, 
    the use of ferrous gluconate is approved for the coloring of ripe 
    olives. Ferrous lactate is a potential substitute for ferrous 
    gluconate. Therefore, to maintain consistency, the agency will refer to 
    ripe olives instead of black olives.
    
    II. Standards for GRAS Affirmation
    
        Under Sec. 170.30 (21 CFR 170.30), general recognition of safety 
    may be based only on the views of experts qualified by scientific 
    training and experience to evaluate the safety of substances added to 
    food. The basis of such views may be either: (1) Scientific procedures, 
    or (2) in the case of a substance used in food prior to January 1, 
    1958, experience based on common use in food (Sec. 170.30(a)). General 
    recognition of safety based upon scientific procedures requires the 
    same quantity and quality of scientific evidence as is required to 
    obtain approval of a food additive regulation and ordinarily is to be 
    based upon published studies, which may be corroborated by unpublished 
    studies and other data and information (Sec. 170.30(b)). General 
    recognition of safety through experience based on common use in food 
    prior to January 1, 1958, may be determined without the quantity or 
    quality of scientific procedures required for approval of a food 
    additive regulation but ordinarily is to be based upon generally 
    available data and information concerning the pre-1958 history of use 
    of the food ingredient (Sec. 170.30(c)). In its petition, Purac 
    America, Inc., relied on the scientific procedures that have been used 
    to support the regulated uses of ferrous lactate in Sec. 184.1311, and 
    on additional submitted published and unpublished data, to establish 
    that ferrous lactate is GRAS for use as a color fixative on ripe 
    olives.
    
    III. Use, Estimated Exposure Levels, and Synthesis of Ferrous 
    Lactate
    
        Ferrous lactate is currently affirmed as GRAS for use as a nutrient 
    supplement under Sec. 184.1311. Because ferrous lactate is used 
    interchangeably with several other iron salts that also may be used as 
    nutrient supplements, FDA considered the exposure to ferrous lactate 
    resulting from its use on ripe olives in relation to total exposure 
    from iron.
        Based on information supplied in the petition, FDA has estimated 
    that the exposure to iron from the consumption of ferrous lactate-
    treated olives would be no greater than 0.14 milligrams per person per 
    day (mg/person/day) (Ref. 1).
    
    [[Page 40318]]
    
    This represents a small contribution to the reference daily intake 
    (RDI) of 18 mg/day for iron (21 CFR 104.20(d)(3)). As ferrous lactate 
    can replace ferrous gluconate for coloring or fixing color in ripe 
    olives, no actual increase in exposure to iron is expected.
        Lactic acid is GRAS (21 CFR 184.1061) and is a ubiquitous component 
    of the human body. FDA has estimated that exposure to lactate from the 
    petitioned use would not contribute significantly to the overall 
    dietary exposure to lactate (Ref. 1).
        Section 184.1311(a) describes ferrous lactate as a greenish-white 
    powder prepared by reacting calcium lactate or sodium lactate with 
    ferrous sulfate or by direct reaction of lactic acid with iron filings. 
    The petitioner described two additional methods for preparing ferrous 
    lactate: (1) Reaction of ferrous chloride with sodium lactate and (2) 
    reaction of ferrous sulfate with ammonium lactate.
        The petitioner also submitted a draft copy of specifications for 
    ferrous lactate that has been incorporated into the 4th edition of the 
    Food Chemicals Codex recently published by the National Academy of 
    Sciences. The agency has reviewed these additional methods of synthesis 
    and specifications for ferrous lactate and has concluded that they are 
    acceptable (Ref. 1).
    
    IV. Safety
    
        FDA discussed the safety of ferrous lactate in a proposal that 
    published in the Federal Register on April 21, 1987 (52 FR 13086). As 
    noted above, ferrous lactate is affirmed as GRAS for use as a nutrient 
    in food under Sec. 184.1311. Ferrous lactate is also recognized as a 
    coloring adjunct and nutrient by the Food and Agriculture Organization/
    World Health Organization and the Joint Expert Committee on Food 
    Additives. Ferrous lactate is listed as a color retention agent in the 
    Registry of Food Additives of the European Communities. Ferrous lactate 
    is also listed by the Spanish Ministry of Health for color fixation of 
    black olives. The petitioner has relied primarily on the above data to 
    support its proposed use of ferrous lactate as a color fixative for 
    ripe olives.
        FDA has considered the information in the petition, along with 
    other available information, concerning ferrous lactate and other iron 
    salts and has concluded that ferrous lactate is safe for use as a color 
    fixative for ripe olives (Ref. 2). This determination is based on the 
    fact that lactate is a normal constituent of food and a normal 
    intermediary metabolite in humans. Ferrous salts are present in many 
    foods, particularly meats and poultry and are used as nutrients in food 
    processing. The exposure to iron from the consumption of ferrous 
    lactate-treated olives represents only a small contribution to the RDI 
    of 18 mg/day for iron.
    
    V. Conclusions on Use of Ferrous Lactate as a Color Fixative on 
    Ripe Olives
    
        FDA has evaluated all of the available information on ferrous 
    lactate. Based on its review, the agency concludes that the data are 
    adequate to demonstrate the safety of ferrous lactate for the 
    petitioned use. Therefore, the agency concludes, based upon scientific 
    procedures, that ferrous lactate is GRAS for use as a color fixative on 
    ripe olives at levels consistent with current good manufacturing 
    practice. The agency is therefore amending Sec. 184.1311 to provide for 
    this use.
        The agency is also amending Sec. 184.1311 to provide for the 
    additional methods of synthesis for ferrous lactate that were discussed 
    above. Additionally, the agency is amending Sec. 184.1311 to require 
    that the ingredient meets the specifications listed in the Food 
    Chemicals Codex. In the existing GRAS regulation for food use of 
    ferrous lactate (Sec. 184.1311), the agency indicated that it was 
    developing specifications for ferrous lactate in cooperation with the 
    National Academy of Sciences. The agency, as noted above, has reviewed 
    the specifications for ferrous lactate that published in the 4th 
    edition of the Food Chemicals Codex and has found them acceptable. 
    Therefore, the agency is amending Sec. 184.1311 to require that ferrous 
    lactate meet the specifications in the Food Chemicals Codex, 4th 
    edition, pages 154 and 155.
    
    VI. Use of Ferrous Lactate as a Color Additive
    
        In the document announcing the filing of Purac America, Inc.'s, 
    GRAS affirmation petition for ferrous lactate, FDA proposed, on its own 
    initiative, to amend the color additive regulations in part 73 (21 CFR 
    part 73) to provide for the safe use of ferrous lactate as a color 
    additive for the coloring of ripe olives. The agency undertook this 
    action because of questions as to whether ferrous lactate, when used 
    for the petitioned purpose, is functioning as a color fixative or as a 
    color additive. Section 721(b)(4) of the Federal Food, Drug, and 
    Cosmetic Act (the act) (21 U.S.C. 379e(b)(4), provides that ``* * * a 
    color additive shall be deemed to be suitable and safe for the purpose 
    of listing under this subsection for use generally in or on food, while 
    there is in effect a published finding of the Secretary declaring such 
    substance exempt from the term `food additive' because of its being 
    generally recognized by qualified experts as safe for its intended use, 
    as provided in section 201(s).'' Therefore, to eliminate any questions 
    with respect to the use of ferrous lactate on ripe olives, the agency 
    proposed to amend part 73 to provide for the safe use of ferrous 
    lactate for the coloring of ripe olives.
        Having concluded that ferrous lactate is GRAS for use as a color 
    fixative on ripe olives, the agency is amending part 73 to provide for 
    the use of ferrous lactate as a color additive for the coloring of ripe 
    olives.
        The agency has also determined that the Food Chemicals Codex 
    specifications for ferrous lactate are acceptable for the color 
    additive use of ferrous lactate in coloring ripe olives, and in the 
    regulation, the agency is requiring that the substance conform to these 
    specifications. Section 721(c) of the act provides that GRAS substances 
    when listed as color additives are exempt from certification. 
    Therefore, ferrous lactate, when used as a color additive for coloring 
    ripe olives, is exempt from certification.
        In accordance with Sec. 71.15 (21 CFR 71.15), the petition and the 
    documents that FDA considered and relied upon in reaching its decision 
    to approve the petition are available for inspection at the Center for 
    Food Safety and Applied Nutrition by appointment with the information 
    contact person listed above. As provided in Sec. 71.15, the agency will 
    delete from the documents any materials that are not available for 
    public disclosure before making the documents available for inspection.
    
    VII. Environmental Effect
    
        The agency has carefully considered the potential environmental 
    effects of this action. FDA has concluded that the action will not have 
    a significant impact on the human environment, and that an 
    environmental impact statement is not required. The agency's finding of 
    no significant impact and the evidence supporting that finding, 
    contained in an environmental assessment, may be seen in the Dockets 
    Management Branch (address above) between 9 a.m. and 4 p.m., Monday 
    through Friday.
    
    VIII. Economic Effects of GRAS Affirmation
    
        FDA has examined the economic implications of this final rule 
    affirming that the use of ferrous lactate is GRAS as a color fixative 
    on ripe olives and of amending Sec. 184.1311 to permit
    
    [[Page 40319]]
    
    additional methods of synthesis for ferrous lactate under Executive 
    Order 12866 and the Regulatory Flexibility Act (Pub. L. 96-354). 
    Executive Order 12866 directs agencies to assess all costs and benefits 
    of available regulatory alternatives and, when regulation is necessary, 
    to select regulatory approaches that maximize net benefits (including 
    potential economic, environmental, public health, and safety effects; 
    distributive impacts; and equity). The Regulatory Flexibility Act 
    requires analyzing options for regulatory relief for small businesses.
        FDA finds that this final rule is not a significant regulatory 
    action as defined by Executive Order 12866. The compliance costs to 
    firms are zero because no current activity is prohibited by affirming 
    the GRAS status of ferrous lactate as a color fixative for ripe olives, 
    or by amending the regulations to permit additional methods of 
    synthesis for ferrous lactate. Because this final rule will not 
    increase the health risks faced by consumers, total health costs are 
    also zero. Potential benefits include the ability to use additional 
    methods to synthesize ferrous lactate and any resources saved by 
    eliminating the need to prepare further petitions to affirm the GRAS 
    status of this substance.
        Affirming that ferrous lactate is GRAS as a color fixative for ripe 
    olives under conditions of current good manufacturing practice and 
    permitting additional methods of synthesis for ferrous lactate will 
    expand the formulation possibilities for food manufacturers, including 
    small businesses. Therefore, in accordance with the Regulatory 
    Flexibility Act, FDA has also determined that this rule will have a 
    positive impact on small businesses.
    
    IX. References
    
        The following references have been placed on display in the Dockets 
    Management Branch (address above) and may be seen by interested persons 
    between 9 a.m. and 4 p.m., Monday through Friday.
    
        1. Memoranda from Chemistry Review Branch, HFS-247, to Direct 
    Additives Branch, HFS-217, dated December 19, 1994, July 28, 1995, 
    and November 21, 1995.
        2. Memorandum from Additives Evaluation Branch no. 1, HFS-226, 
    to Direct Additives Branch, HFS-217, dated September 9, 1993.
    
    X. Objections to Sec. 73.165
    
        Any person who will be adversely affected by new Sec. 73.165 may at 
    any time on or before September 3, 1996, file with the Dockets 
    Management Branch (address above) written objections thereto. Each 
    objection shall be separately numbered, and each numbered objection 
    shall specify with particularity the provisions of the regulation to 
    which objection is made and the grounds for the objection. Each 
    numbered objection on which a hearing is requested shall specifically 
    so state. Failure to request a hearing for any particular objection 
    shall constitute a waiver of the right to a hearing on that objection. 
    Each numbered objection for which a hearing is requested shall include 
    a detailed description and analysis of the specific factual information 
    intended to be presented in support of the objection in the event that 
    a hearing is held. Failure to include such a description and analysis 
    for any particular objection shall constitute a waiver of the right to 
    a hearing on the objection. Three copies of all documents shall be 
    submitted and shall be identified with the docket number found in 
    brackets in the heading of this document. Any objections received in 
    response to the regulation may be seen in the Dockets Management Branch 
    between 9 a.m. and 4 p.m., Monday through Friday. FDA will publish 
    notice of the objections that the agency has received or lack thereof 
    in the Federal Register.
    
    List of Subjects
    
    21 CFR Part 73
    
        Color additives, Cosmetics, Drugs, Medical devices.
    
    21 CFR Part 184
    
        Food ingredients.
        Therefore, under the Federal Food, Drug, and Cosmetic Act and under 
    authority delegated to the Commissioner of Food and Drug and 
    redelegated to the Director, Center for Food Safety and Applied 
    Nutrition, 21 CFR parts 73 and 184 are amended as follows:
    
    PART 73--LISTING OF COLOR ADDITIVES EXEMPT FROM CERTIFICATION
    
        1. The authority citation for 21 CFR part 73 continues to read as 
    follows:
    
        Authority: Secs. 201, 401, 402, 403, 409, 501, 502, 505, 601, 
    602, 701, 721 of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 
    321, 341, 342, 343, 348, 351, 352, 355, 361, 362, 371, 379e).
    
        2. New Sec. 73.165 is added to subpart A to read as follows:
    
    
    Sec. 73.165  Ferrous lactate.
    
        (a) Identity. The color additive ferrous lactate is the ferrous 
    lactate defined in Sec. 184.1311 of this chapter.
        (b) Specifications. Ferrous lactate shall meet the specifications 
    given in the Food Chemicals Codex, 4th ed. (1996), pp. 154 to 155, 
    which is incorporated by reference in accordance with 5 U.S.C. 552(a) 
    and 1 CFR part 51. Copies are available from the National Academy 
    Press, 2101 Constitution Ave. NW., Washington, DC 20418, or may be 
    examined at the Center for Food Safety and Applied Nutrition's Library, 
    200 C St. SW., rm. 3321, Washington, DC, or at the Office of the 
    Federal Register, 800 North Capitol St. NW., suite 700, Washington, DC.
        (c) Uses and restrictions. Ferrous lactate may be safely used in 
    amounts consistent with good manufacturing practice for the coloring of 
    ripe olives.
        (d) Labeling. The label of the color additive shall conform to the 
    requirements of Sec. 70.25 of this chapter.
        (e) Exemption from certification. Certification of this color 
    additive is not necessary for the protection of the public health, and 
    therefore batches thereof are exempt from the certification 
    requirements of section 721(c) of the Federal Food, Drug, and Cosmetic 
    Act (the act).
    
    PART 184--DIRECT FOOD SUBSTANCES AFFIRMED AS GENERALLY RECOGNIZED 
    AS SAFE
    
        Authority: Secs. 201, 402, 409, 701 of the Federal Food, Drug, 
    and Cosmetic Act (21 U.S.C. 321, 342, 348, 371).
    
        3. Section 184.1311 is amended by revising paragraphs (a), (b), and 
    (c) to read as follows:
    
    
    Sec. 184.1311  Ferrous lactate.
    
        (a) Ferrous lactate (iron (II) lactate, C6H10FeO6, 
    CAS Reg. No. 5905-52-2) in the trihydrate form is a greenish-white 
    powder or crystalline mass. It is prepared by reacting calcium lactate 
    or sodium lactate with ferrous sulfate, direct reaction of lactic acid 
    with iron filings, reaction of ferrous chloride with sodium lactate, or 
    reaction of ferrous sulfate with ammonium lactate.
        (b) The ingredient meets the specifications of the Food Chemicals 
    Codex, 4th ed. (1996), pp. 154 to 155, which is incorporated by 
    reference in accordance with 5 U.S.C. 552(a) and 1 CFR part 51. Copies 
    are available from the National Academy Press, 2101 Constitution Ave. 
    NW., Washington, DC 20418, or may be examined at the Center for Food 
    Safety and Applied Nutrition's library, 200 C St. SW., rm. 3321, 
    Washington, DC, or at the Office of the Federal Register, 800 North 
    Capitol St. NW., suite 700, Washington, DC.
        (c) In accordance with Sec. 184.1(b)(1), the ingredient is used in 
    food as a nutrient supplement as defined in
    
    [[Page 40320]]
    
    Sec. 170.3(o)(20) of this chapter and as a color fixative for ripe 
    olives, with no other limitation other than current good manufacturing 
    practice. The ingredient may also be used in infant formula in 
    accordance with section 412(g) of the Federal Food, Drug, and Cosmetic 
    Act (the act) (21 U.S.C. 350a(g)) or with regulations promulgated under 
    section 412(a)(2) of the act (21 U.S.C. 350a(a)(2)).
    * * * * *
    
        Dated: July 19, 1996.
    Janice F. Oliver,
    Deputy Director for Systems and Support, Center for Food Safety and 
    Applied Nutrition.
    [FR Doc. 96-19305 Filed 8-1-96; 8:45 am]
    BILLING CODE 4160-01-F