99-13254. Sumitomo Chemical Co. Ltd.; Filing of Food Additive Petition  

  • [Federal Register Volume 64, Number 101 (Wednesday, May 26, 1999)]
    [Notices]
    [Page 28501]
    From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
    [FR Doc No: 99-13254]
    
    
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    DEPARTMENT OF HEALTH AND HUMAN SERVICES
    
    Food And Drug Administration
    [Docket No. 99F-1422]
    
    
    Sumitomo Chemical Co. 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 
    Sumitomo Chemical Co., Ltd. has filed a petition proposing that the 
    food additive regulations be amended to provide for the expanded safe 
    use of 2,4-di-tert-pentyl-6-[1-(3,5-di-tert-pentyl-2-
    hydroxyphenyl)ethyl]phenyl acrylate as an antioxidant and/or stabilizer 
    for polypropylene, polystyrene, rubber modified polystyrene, and 
    styrene block copolymers intended for use in contact with food.
    
    FOR FURTHER INFORMATION CONTACT: Vir D. Anand, Center for Food Safety 
    and Applied Nutrition (HFS-215), Food and Drug Administration, 200 C 
    St. SW., Washington, DC 20204, 202-418-3081.
    
    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 9B4661) has been filed by Sumitomo Chemical Co., 
    Ltd., c/o Keller and Heckman LLP, 1001 G St. NW., suite 500 West, 
    Washington, DC 20001. 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 expanded safe use of 2,4-
    di-tert-pentyl-6-[1-(3,5-di-tert-pentyl-2-hydroxyphenyl)ethyl]phenyl 
    acrylate as an antioxidant and/or stabilizer for polypropylene, 
    polystyrene, rubber modified polystyrene, and styrene block copolymers 
    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.
    
        Dated: May 5, 1999.
    Alan M. Rulis,
    Director, Office of Premarket Approval, Center for Food Safety and 
    Applied Nutrition.
    [FR Doc. 99-13254 Filed 5-25-99; 8:45 am]
    BILLING CODE 4160-01-F
    
    
    

Document Information

Published:
05/26/1999
Department:
Food and Drug Administration
Entry Type:
Notice
Action:
Notice.
Document Number:
99-13254
Pages:
28501-28501 (1 pages)
Docket Numbers:
Docket No. 99F-1422
PDF File:
99-13254.pdf