La. Admin. Code tit. 7 § XVII-115
Current through Register Vol. 50, No. 9, September 20, 2024
Section XVII-115 - Drug and Feed AdditivesA. Prior to approval of a registration application and/or approval of a label for commercial feed which contains 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.B. Satisfactory evidence of safety and efficacy of a commercial feed may be:1. when the commercial feed contains such additives, the use of which conforms to the requirements of the applicable regulation in the Code of Federal Regulations, Title 21, or which are prior sanctioned or informal review sanctioned or generally recognized as safe for such use; or2. when the commercial feed is itself a drug as defined in R.S. 3:1391(3) and is generally recognized 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).La. Admin. Code tit. 7, § XVII-115
Promulgated by the Department of Agriculture, Feed Commission, LR 11:223 (March 1985), amended by the Department of Agriculture and Forestry, Feed, Fertilizer, and Agricultural Liming Commission, LR 38:2524 (October 2012).AUTHORITY NOTE: Promulgated in accordance with R.S. 3:1394 and R.S. 3:1392.