21 C.F.R. · Food and Drugs
21 C.F.R. § 516.155

Labeling of indexed drugs.

Title 21 C.F.R. ● ACTIVE Primary Source
Regulatory Text

21 C.F.R. § 516.155 — Labeling of indexed drugs.

§ 516.155 Labeling of indexed drugs. (a) The labeling of an indexed drug that is found to be eligible for indexing under § 516.129(c)(7)(i) shall state, prominently and conspicuously: “NOT APPROVED BY FDA.—Legally marketed as an FDA indexed product. Extra-label use is prohibited.” “This product is not to be used in animals intended for use as food for humans or other animals.” (b) The labeling of an indexed drug that was found to be eligible for indexing for use in an early, non-food life stage of a food-producing minor species animal, under § 516.129(c)(7)(ii), shall state, prominently and conspicuously: “NOT APPROVED BY FDA.—Legally marketed as an FDA indexed product. Extra-label use is prohibited.” (c) The labeling of an indexed drug shall contain such other information as may be prescribed in the index listing.

Source: ecfr.gov · govinfo.gov — public domain Official Source ↗
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21 C.F.R. § 516.155
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The regulatory text of 21 C.F.R. § 516.155 is reproduced from the official Code of Federal Regulations as published by the Office of the Federal Register and the National Archives and Records Administration.
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