Ga. Comp. R. & Regs. R. 40-5-4-.01 - Drug and Feed Additives
(1)
Prior to approval of the label for commercial feed which contain additives
(including drugs, other special purpose additives, or non-nutritive 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.
(2) Satisfactory
evidence of safety and efficacy of a commercial feed may be:
(a) When the commercial feed contains such
additives, the use of which conforms to the requirements of the applicable
regulation in the most current Code of Federal Regulations, Title 21, or which
are "prior sanctioned" or "informal review sanctioned" or "generally recognized
as safe" for such use, or
(b) When
the commercial feed is itself a drug as defined in Section
2-13-1(6) of the
Act and is generally recognize d as safe and effective for the labeled use or
is marketed subject to an application approved by the Food and Drug
Administration under Title 21 U.S.C. 360(b),
or
(c) When one of the purposes for
feeding a commercial feed is to impart immunity (that is to act through some
immunological process) the constituents imparting immunity have been approved
for the purpose through the Federal Virus, Serum and Toxins Act of 1913, as
amended, or
(d) When the commercial
feed is a direct fed microbial product and:
1.
The product meets the particular fermentation product definition; and
2. The microbial content statement, as
expressed in the labeling, is limited to the following: "Contains a source of
live (viable) naturally occurring microorganisms." This statement shall appear
on the label; and
3. The source is
stated with a corresponding guarantee expressed in accordance with Regulation
40-5-2-.03(7).
Notes
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