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Code · REGISTER · 2003-08-21 · Food and Drug Administration, HHS · Notices

Notices. Notice

271 words·~1 min read·/register/2003/08/21/03-21396·

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BILLING CODE 6210-01-S DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. 2003F-0370] Unilever United States, Inc.; Filing of Food Additive Petition AGENCY: Food and Drug Administration, HHS. ACTION: Notice. SUMMARY: The Food and Drug Administration
(FDA)is announcing that Unilever United States, Inc., has filed a petition proposing that the food additive regulations be amended to provide for the safe use of vitamin D <sup>3</sup> as a nutrient supplement in certain foods for special dietary use, such as meal replacement products and snack replacement products. FOR FURTHER INFORMATION CONTACT: Judith L. Kidwell, Center for Food Safety and Applied Nutrition (HFS-265), Food and Drug Administration, 5100 Paint Branch Pkwy., College Park, MD 20740-3835, 202-418-3354. 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 No. 3A4746) has been filed by Unilever United States, Inc., 390 Park Ave., New York, NY 10022-4698. The petition proposes to amend the food additive regulations in § 172.380 *Vitamin D* <sup>3</sup> (21 CFR 172.380) to provide for the safe use of vitamin D <sup>3</sup> in certain foods for special dietary use, such as meal replacement products and snack replacement products. 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 1, 2003. Laura M. Tarantino, Acting Director, Office of Food Additive Safety, Center for Food Safety and Applied Nutrition. [FR Doc. 03-21396 Filed 8-20-03; 8:45 am]
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