95-10539. GNT Gesellshaft fur Nahrungsmitteltechnologie mbH; Filing of Color Additive Petition  

  • [Federal Register Volume 60, Number 82 (Friday, April 28, 1995)]
    [Notices]
    [Page 20997]
    From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
    [FR Doc No: 95-10539]
    
    
    
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    DEPARTMENT OF HEALTH AND HUMAN SERVICES
    Food and Drug Administration
    [Docket No. 95C-0091]
    
    
    GNT Gesellshaft fur Nahrungsmitteltechnologie mbH; Filing of 
    Color Additive Petition
    
    AGENCY: Food and Drug Administration, HHS.
    
    ACTION: Notice.
    
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    SUMMARY: The Food and Drug Administration (FDA) is announcing that GNT 
    Gesellshaft fur Nahrungsmitteltechnologie mbH has filed a petition 
    proposing that the color additive regulations be amended to provide for 
    the safe use of dried fruit juice color additive, dried vegetable juice 
    color additive, and vegetable juice color additive prepared by water 
    infusion of the dried vegetable.
    
    FOR FURTHER INFORMATION CONTACT: Aydin Orstan, Center for Food Safety 
    and Applied Nutrition (HFS-217), Food and Drug Administration, 200 C 
    St. SW., Washington, DC 20204, 202-418-3076.
    
    SUPPLEMENTARY INFORMATION: Under the Federal Food, Drug, and Cosmetic 
    Act (sec. 721(b)(5) (21 U.S.C. 379e(b)(5))), notice is given that a 
    color additive petition (CAP 5C0245) has been filed by GNT Gesellshaft 
    fur Nahrungsmitteltechnologie mbH, c/o Burditt & Radzius, Chtd., 333 
    West Wacker Dr., suite 2600, Chicago, IL 60606-1218. The petition 
    proposes to amend the color additive regulations in Sec. 73.250 Fruit 
    juice (21 CFR 73.250) to provide for the safe use of dried fruit juice 
    color additive and in Sec. 73.260 Vegetable juice (21 CFR 73.260) to 
    provide for the safe use of dried vegetable juice color additive, and 
    vegetable juice color additive prepared by water infusion of the dried 
    vegetable.
        The agency has determined under 21 CFR 25.24(a)(9) that this action 
    is of a 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: April 20, 1995.
    Alan M. Rulis,
    Acting Director, Office of Premarket Approval, Center for Food Safety 
    and Applied Nutrition.
    [FR Doc. 95-10539 Filed 4-27-95; 8:45 am]
    BILLING CODE 4160-01-F
    
    

Document Information

Published:
04/28/1995
Department:
Food and Drug Administration
Entry Type:
Notice
Action:
Notice.
Document Number:
95-10539
Pages:
20997-20997 (1 pages)
Docket Numbers:
Docket No. 95C-0091
PDF File:
95-10539.pdf