Section R3-3-910. Drug and Feed Additives

A.      Drug and feed additive approval.

1.        Before a label is approved by the Associate Director for commercial feed containing additives (including drugs, other special purpose additives, or non-nutritive addi- tives), the distributor may be required to submit evidence demonstrating the safety and efficacy of the commercial feed when used according to the label directions if the material is not recognized as a commercial feed.

2.        If a complaint has been filed with the Department, the distributor may be required to submit evidence demon- strating the safety and efficacy of the commercial feed when used according to the label directions.

B.       Evidence of safety and efficacy of a commercial feed may be:

1.        If the commercial feed containing additives conforms to the requirements of “Food Additives Permitted in Feed and Drinking” in the Official Publication, which is incor- porated by reference, on file with the Office of the Secre- tary of State, and does not included any later amendments or editions; or

2.        If the commercial feed is a substance generally recog- nized as safe and is defined in the Official Publication or listed as a “Substances Generally Recognized as Safe in Animal Feeds” in the Official Publication, which is incor- porated by reference, on file with the Office of the Secre- tary of State, and does not include any later amendments or editions.

Historical Note

Former rule X; Former Section R3-3-50 repealed, new Section 3-3-50 adopted effective January 12, 1978 (Supp.

78- 1). Amended effective July 20, 1984 (Supp. 84-4). Section R3-3-910 renumbered from R3-3-50 (Supp. 91- 4). Amended by final rulemaking at 5 A.A.R. 4419, effec- tive November 3, 1999 (Supp. 99-4).