98-32023. Solvay S.A.; Filing of Food Additive Petition  

  • [Federal Register Volume 63, Number 231 (Wednesday, December 2, 1998)]
    [Notices]
    [Page 66549]
    From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
    [FR Doc No: 98-32023]
    
    
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    DEPARTMENT OF HEALTH AND HUMAN SERVICES
    
    Food and Drug Administration
    [Docket No. 98F-1034]
    
    
    Solvay S.A.; 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 
    Solvay S.A., has filed a petition proposing that the food additive 
    regulations be amended to provide for the expanded safe use of 
    naphthalene sulfonic acid-formaldehyde condensate, sodium salt as an 
    emulsifier in vinylidene chloride copolymer or homopolymer coatings 
    applied to polypropylene polymer films and polyethylene phthalate 
    polymer films 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 8B4634) has been filed by Solvay S.A., 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. 178.3400 Emulsifiers and/or surface active agents (21 CFR 
    178.3400) to provide for the expanded safe use of naphthalene sulfonic 
    acid-formaldehyde condensate, sodium salt as an emulsifier in 
    vinylidene chloride copolymer or homopolymer coatings applied to 
    polypropylene polymer films and polyethylene phthalate polymer films 
    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: November 16, 1998.
    Laura M. Tarantino,
    Acting Director, Office of Premarket Approval, Center for Food Safety 
    and Applied Nutrition.
    [FR Doc. 98-32023 Filed 12-1-98; 8:45 am]
    BILLING CODE 4160-01-F
    
    
    

Document Information

Published:
12/02/1998
Department:
Food and Drug Administration
Entry Type:
Notice
Action:
Notice.
Document Number:
98-32023
Pages:
66549-66549 (1 pages)
Docket Numbers:
Docket No. 98F-1034
PDF File:
98-32023.pdf