96-31860. Indirect Food Additives: Adjuvants, Production Aids, and Sanitizers  

  • [Federal Register Volume 61, Number 242 (Monday, December 16, 1996)]
    [Rules and Regulations]
    [Pages 65943-65944]
    From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
    [FR Doc No: 96-31860]
    
    
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    DEPARTMENT OF HEALTH AND HUMAN SERVICES
    21 CFR Part 178
    
    [Docket No. 93F-0318]
    
    
    Indirect Food Additives: Adjuvants, Production Aids, and 
    Sanitizers
    
    AGENCY: Food and Drug Administration, HHS.
    
    ACTION: Final rule.
    
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    SUMMARY: The Food and Drug Administration (FDA) is amending the food 
    additive regulations to provide for the safe use of 2-[[2,4,8,10-
    tetrakis(1,1-dimethylethyl)dibenzo[d,f][1,3,2]-dioxaphosphepin-6-
    yl]oxy]-N, N-bis[2-[[2,4,8,10-tetrakis(1,1-dimethylethyl)dibenzo[d,f] 
    [1,3,2]dioxaphosphepin-6-yl]oxy]ethyl]ethanamine as a process 
    stabilizer in high density polyethylene and polypropylene polymers 
    intended for use in contact with food. This action is in response to a 
    petition filed by Ciba-Geigy Corp.
    
    DATES: Effective December 16, 1996; written objections and requests for 
    a hearing by January 15, 1997.
    
    ADDRESSES: Submit written objections to the Dockets Management Branch 
    (HFA-305), Food and Drug Administration, 12420 Parklawn Dr., rm. 1-23, 
    Rockville, MD 20857.
    
    FOR FURTHER INFORMATION CONTACT: Vir D. Anand, Center for Food Safety 
    and Applied Nutrition (HFS-216), Food and Drug Administration, 200 C 
    St. SW., Washington, DC 20204, 202-418-3081.
    
    SUPPLEMENTARY INFORMATION: In a notice published in the Federal 
    Register of October 4, 1993 (58 FR 51631), FDA announced that a food 
    additive petition (FAP 3B4398) had been filed by Ciba-Geigy Corp., 
    Seven Skyline Dr., Hawthorne, NY 10532. The petition proposed to amend 
    the food additive regulations in Sec. 178.2010 Antioxidants and/or 
    stabilizers for polymers (21 CFR 178.2010) to provide for the safe use 
    of 2-[[2,4,8,10-tetrakis(1,1-dimethylethyl)dibenzo 
    [d,f][1,3,2]dioxaphosphepin-6-yl]oxy]-N, N-bis[2-[[2,4,8,10-
    tetrakis(1,1-dimethylethyl)dibenzo [d,f][1,3,2]dioxaphosphepin-6-
    yl]oxy]ethyl]ethanamine as a process stabilizer in high density 
    polyethylene and polypropylene polymers complying with 21 CFR 177.1520 
    intended for use in contact with food.
        FDA has evaluated data in the petition and other relevant material. 
    The agency concludes that the proposed use of the additive is safe, 
    that the additive will achieve its intended technical effect, and that 
    the regulations in Sec. 178.2010 should be amended as set forth below.
        In accordance with Sec. 171.1(h) (21 CFR 171.1(h)), the petition 
    and the documents that FDA considered and relied upon in reaching its 
    decision to
    
    [[Page 65944]]
    
    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. 171.1(h), the agency 
    will delete from the documents any materials that are not available for 
    public disclosure before making the documents available for inspection.
        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.
        Any person who will be adversely affected by this regulation may at 
    any time on or before January 15, 1997 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.
    
    List of Subjects in 21 CFR Part 178
    
        Food additives, Food packaging.
        Therefore, under the Federal Food, Drug, and Cosmetic Act and under 
    authority delegated to the Commissioner of Food and Drugs and 
    redelegated to the Director, Center for Food Safety and Applied 
    Nutrition, 21 CFR part 178 is amended as follows:
    
    PART 178--INDIRECT FOOD ADDITIVES: ADJUVANTS, PRODUCTION AIDS, AND 
    SANITIZERS
    
        1. The authority citation for 21 CFR part 178 continues to read as 
    follows:
    
        Authority: Secs. 201, 402, 409, 721 of the Federal Food, Drug, 
    and Cosmetic Act (21 U.S.C. 321, 342, 348, 379e).
    
        2. Section 178.2010 is amended in the table in paragraph (b) by 
    revising the entry for ``2-[[2,4,8,10-tetrakis(1,1-
    dimethylethyl)dibenzo [d,f][1,3,2]dioxaphosphepin-6-yl]oxy]-N, N-bis[2-
    [[2,4,8,10-tetrakis(1,1-dimethylethyl)dibenzo 
    [d,f][1,3,2]dioxaphosphepin-6-yl]oxy]ethyl]ethanamine'' under the 
    heading ``Limitations'' to read as follows:
    
    Sec. 178.2010  Antioxidants and/or stabilizers for polymers.
    
    * * * * *
        (b) * * *
    
                                                                            
    ------------------------------------------------------------------------
                 Substances                          Limitations            
    ------------------------------------------------------------------------
      *                    *                    *                    *      
                       *                    *                    *          
    2-[[2,4,8,10-Tetrakis(1,1-           For use only at levels not to      
     dimethylethyl)dibenzo[d,f][1,3,2]-   exceed 0.075 percent by weight of 
     dioxaphosphepin-6-yl]oxy]-N,N-       olefin copolymers complying with  
     bis[2-[[2,4,8,10-tetrakis(1,1-       Sec.  177.1520(c) of this chapter,
     dimethylethyl)dibenzo[d,f][1,3,2]d   items 1.1, 1.2, 1.3, 2.1, 2.2, or 
     ioxaphosphepin-6-                    2.3: Provided, That the density of
     yl]oxy]ethyl]ethanamine (CAS Reg.    the olefin polymers complying with
     No. 80410-33-9).                     items 2.1, 2.2, or 2.3 is not less
                                          than 0.94 gram per cubic          
                                          centimeter: And further provided, 
                                          That the finished polymers contact
                                          food only of Types I, II, IV-B, VI-
                                          A, VI-B, VII-B, and VIII described
                                          in Table 1, of Sec.  176.170(c) of
                                          this chapter, under conditions of 
                                          use B through H described in Table
                                          2 of Sec.  176.170(c) of this     
                                          chapter and food only of Types    
                                          III, IV-A, V, VI-C, VII-A, and IX 
                                          described in Table 1 of Sec.      
                                          176.170(c) of this chapter, under 
                                          conditions of use C through G     
                                          described in Table 2 of Sec.      
                                          176.170(c) of this chapter.       
      *                    *                    *                    *      
                       *                    *                    *          
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        Dated: November 27, 1996.
    Fred R. Shank,
    Director, Center for Food Safety and Applied Nutrition.
    [FR Doc. 96-31860 Filed 12-13-96; 8:45 am]
    BILLING CODE 4160-01-F
    
    
    

Document Information

Effective Date:
12/16/1996
Published:
12/16/1996
Department:
Health and Human Services Department
Entry Type:
Rule
Action:
Final rule.
Document Number:
96-31860
Dates:
Effective December 16, 1996; written objections and requests for a hearing by January 15, 1997.
Pages:
65943-65944 (2 pages)
Docket Numbers:
Docket No. 93F-0318
PDF File:
96-31860.pdf
CFR: (1)
21 CFR 178.2010