This Administrative Order pursuant to R.A. No. 3720 -as amended by Executive Order No. 175, known as the “Foods, Drugs and Devices and Cosmetics Act”; R.A. 1071, an Act to regulate the sale of veterinary biologics and medicinal preparation and R.A. 3101, an Act authorizing the Director of Animal Industry, subject to the approval of the Secretary of Agriculture and Natural Resources to promulgate regulations for the preparation, sale, traffic in shipment and importation of viruses, sera, toxins or analogous products used for the treatment of domestic animals- establishes the following requirements for the labelling of veterinary drugs and products for the information, guidance and compliance of all concerned. It specifies the minimum mandatory information that shall be included in the labelling materials on the immediate container and package and other printed materials that are made available with the veterinary drug and product at the time of purchase and/or where the veterinary drug and product is used, such as the outer wrapper cartons, leaflet/package insert accompanying the product, which provide the accurate and necessary detailed information for the identification and proper use of the veterinary drug and product.
Philippines · 1991-04-15