7 Pa. Code § 71.8 - Drug and feed additives
(a) Prior
to approval of a facility registration for commercial feed which contains
additives, including drugs, other special purpose additives or nonnutritive
additives, the distributor may be required to submit evidence to prove the
safety and efficacy of the commercial feed when used according to the
directions furnished on the label.
(b) Satisfactory evidence of safety and
efficacy of a commercial feed may consist of either of the following:
(1) When the commercial feed contains such
additives, the use of which conforms to the requirements of the applicable
regulation in Title 21 of the Code of Federal Regulations, or
which are "prior sanctioned" or "generally recognized as safe" for such
use.
(2) When the commercial feed
is itself a drug as defined in section 3(16) of the act (3 P. S. §
58.3(16)) and is generally
recognized as safe and effective for the labeled use or is marketed subject to
an application approved by the United States Food and Drug Administration under
the Federal Food, Drug and Cosmetic Act, section 302, 76 Stat. 794,
21 U.S.C.A. §
360(b).
Notes
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