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ビジネス · 1997/9/231 分で読めます

Food Labeling; Statement of Identity, Nutrition Labeling and Ingredient Labeling of Dietary Supplements; Compliance Policy Guide, Revocation

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概要

The Food and Drug Administration (FDA) is amending its food labeling regulations to establish requirements for the identification of dietary supplements and for their nutrition labeling and ingredient labeling in response to the Dietary Supplement Health and Education Act of 1994 (the DSHEA). FDA is also responding to a citizen petition from the Council for Responsible Nutrition on type size requirements for these products. In addition, FDA is announcing the revocation of Compliance Policy Guide 530.400 (CPG 7121.02) entitled ``Vitamin Products for Human Use--Low Potency'' to eliminate inconsistencies with the new labeling requirements.

情報源の原言語: Federal Register — Food and Drug Administration原文の発表を開く →

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