1 CRR-NY 257.8NY-CRR
1 CRR-NY 257.8
1 CRR-NY 257.8
257.8 Drugs and other additives.
(a) The commissioner may require approval of any labeling on or for any commercial feed which contains any drug or other additive (including any special-purpose or nonnutritive additive).
(b) Prior to approval of any application for registration, as provided in section 129(1) or (2) of the law, or prior to approval by the commissioner of any labeling for any commercial feed which contains any additive, the commissioner may require the applicant or registrant to submit evidence to prove the safety and efficacy of such feed when used according to the directions furnished on the labeling.
(c) Evidence of the safety and efficacy of any commercial feed shall be deemed satisfactory for the purposes of this section when:
(1) the commercial feed contains such additives, the use of which conforms to the requirements of applicable regulations promulgated pursuant to the Federal Food, Drug and Cosmetic Act, or which are “prior sanctioned” or “generally recognized as safe” for such use pursuant to the provisions of such act; or
(2) the commercial feed is itself a drug as defined in the law and is generally recognized as safe and effective for the labeled use or is marketed subject to an application approved by the Federal Food and Drug Administration under title 21 of USC 355, 357 or 360(b).
1 CRR-NY 257.8
Current through August 31, 2021
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