Current through Register Vol. 49, No. 6, March 15, 2024
1)
Office of the Federal Register National Archives and Records Administration,
Code of Federal Regulations Title 21 (Washington: U.S. Government Printing
Office, 1995); and
2)
Office of the Law Revision Counsel of the House of Representatives,
U.S. Code Title 21, 360(b) (Washington: U.S. Government Printing Office,
1995).
In accordance with section
536.031(4),
RSMo, the full text of material incorporated
by reference will be made available to any interested person at the Office of
the Secretary of State and the headquarters of the adopting state
agency.
(1) An artificial
color may be used in a pet food only if it has been shown to be harmless to
pets. The permanent or provisional listing of an artificial color in the United
States Food and Drug Regulations,
2 CSR
70-30.085, as safe for use, together with the
conditions, limitations, and tolerances, if any, incorporated therein, shall be
deemed to be satisfactory evidence that the color is, when used pursuant to
these regulations, harmless to pets.
(2) Prior to approval of a registration
application and/or approval of a label for pet food, 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 pet food, when used according to directions furnished on the
label. Satisfactory evidence of the safety and efficacy of a pet food may be-
(A) When the pet food contains these
additives, the use of which conforms to the requirements of the applicable
regulation in the Code of Federal Regulations, Title 21,
2 CSR
70-30.085, or which are "prior sanctioned" or
"Generally Recognized As Safe" for such use; or
(B) When the pet food itself is a drug as
defined in section
266.160(7), RSMo and
is generally recognized as safe and effective for label use or is marketed
subject to an application approved by the Food and Drug Administration under
Title 21, U.S.C. 360(b)
2 CSR
70-30.085; and
(C) The medicated labeling format recommended
by the Association of American Feed Control Officials,
2 CSR 70-30.020
shall be used to assure that adequate labeling is provided.
*Original authority 1972 amended 1993,
1995.
