99-23682. American Ingredients Co.; Filing of Food Additive Petition  

  • [Federal Register Volume 64, Number 176 (Monday, September 13, 1999)]
    [Notices]
    [Pages 49495-49496]
    From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
    [FR Doc No: 99-23682]
    
    
    =======================================================================
    -----------------------------------------------------------------------
    
    DEPARTMENT OF HEALTH AND HUMAN SERVICES
    
    Food and Drug Administration
    [Docket No. 99F-3087]
    
    
    American Ingredients Co.; Filing of Food Additive Petition
    
    AGENCY: Food and Drug Administration, HHS.
    
    ACTION: Notice.
    
    -----------------------------------------------------------------------
    
    SUMMARY: The Food and Drug Administration (FDA) is announcing that 
    American Ingredients Co. has filed a petition proposing that the food 
    additive regulations be amended to provide for the safe use of sodium 
    stearoyl lactylate as an emulsifier,
    
    [[Page 49496]]
    
    stabilizer, and texturizer in cream liqueur drinks.
    
    FOR FURTHER INFORMATION CONTACT: Mary E. LaVecchia, Center for Food 
    Safety and Applied Nutrition (HFS-215), Food and Drug Administration, 
    200 C St. SW., Washington, DC 20204, 202-418-3072.
    
    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 9A4684) has been filed by American Ingredients 
    Co., 3947 Broadway, Kansas City, MO 64111. The petition proposes to 
    amend the food additive regulations in Sec. 172.846 Sodium stearoyl 
    lactylate (21 CFR 172.846) to provide for the expanded safe use of 
    sodium stearoyl lactylate as an emulsifier, stabilizer, and texturizer 
    in cream liqueur drinks.
        The agency has determined under 21 CFR 25.32(k) 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: August 31, 1999.
    Alan M. Rulis,
    Director, Office of Premarket Approval, Center for Food Safety and 
    Applied Nutrition.
    [FR Doc. 99-23682 Filed 9-10-99; 8:45 am]
    BILLING CODE 4160-01-F
    
    
    

Document Information

Published:
09/13/1999
Department:
Food and Drug Administration
Entry Type:
Notice
Action:
Notice.
Document Number:
99-23682
Pages:
49495-49496 (2 pages)
Docket Numbers:
Docket No. 99F-3087
PDF File:
99-23682.pdf