97-27532. Yoshitomi Fine Chemicals, Ltd.; Filing of Food Additive Petition  

  • [Federal Register Volume 62, Number 201 (Friday, October 17, 1997)]
    [Notices]
    [Pages 54117-54118]
    From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
    [FR Doc No: 97-27532]
    
    
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    DEPARTMENT OF HEALTH AND HUMAN SERVICES
    
    Food and Drug Administration
    [Docket No. 97F-0421]
    
    
    Yoshitomi Fine Chemicals, Ltd.; Filing of Food Additive Petition
    
    AGENCY: Food and Drug Administration, HHS.
    
    ACTION: Notice.
    
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    SUMMARY: The Food and Drug Administration (FDA) is announcing that 
    Yoshitomi Fine Chemicals, Ltd., has filed a petition proposing that the 
    food additive regulations be amended to provide for the safe use of Di-
    tert-butylcresyl phosphonite condensation product with biphenyl for use 
    as an antioxidant and/or stabilizer for olefin polymers intended for 
    use in contact with food.
    
    FOR FURTHER INFORMATION CONTACT: Hortense S. Macon, Center for Food 
    Safety and Applied Nutrition (HFS-205), Food and Drug Administration, 
    200 C St. SW., Washington, DC 20204, 202-418-3086.
    
    SUPPLEMENTARY INFORMATION: Under the Federal Food, Drug, and Cosmetic 
    Act (sec. 409(b)(5) (21 U.S.C. 348(b)(5))), notice is given that a food 
    additive petition (FAP 7B4557) has been filed by Yoshitomi Fine 
    Chemicals, Ltd., 6-9 Hiranomachi 2-chome, Chuo-ku, Osaka 541, Japan. 
    The petition proposes 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 Di-tert-butylcresyl 
    phosphonite condensation product with biphenyl,produced by the 
    condensation of 2,4-di-tert-butylcresol with the Friedel-Crafts 
    addition product of phosphorous trichloride and biphenyl,for use as an 
    antioxidant and/or stabilizer for olefin polymers intended for use in 
    contact with food.
        The agency has determined under 21 CFR 25.32(i) that this action is 
    of the type that does not individually or cumulatively have a 
    significant effect on the human environment. Therefore, neither an 
    environmental assessment nor an environmental impact statement is 
    required.
    
    
    [[Page 54118]]
    
    
        Dated: September 23, 1997.
    Alan M. Rulis,
    Director, Office of Premarket Approval, Center for Food Safety and 
    Applied Nutrition.
    [FR Doc. 97-27532 Filed 10-16-97; 8:45 am]
    BILLING CODE 4160-01-F
    
    
    

Document Information

Published:
10/17/1997
Department:
Food and Drug Administration
Entry Type:
Notice
Action:
Notice.
Document Number:
97-27532
Pages:
54117-54118 (2 pages)
Docket Numbers:
Docket No. 97F-0421
PDF File:
97-27532.pdf