Due to the limitation of packaging size, ampoules, penicillin bottles and other injections or oral products cannot indicate all the above contents, and items can be appropriately reduced, but at least the name, content specifications and production batch number of the veterinary drug must be indicated. Article 6 The outer packaging label must indicate the animal identification, veterinary drug name, main ingredients, indications (or functional indications), usage and dosage, contents/packaging specifications, approval number or certificate number of the registration license for imported veterinary drugs, production date, production batch number, expiration date, drug withdrawal period, storage and packaging quantity, information of production enterprises, etc. Article 7 The label of veterinary API must indicate the name of veterinary drug, packaging specifications, production batch number, production date, expiration date, storage, approval number, transportation precautions or other signs, information of production enterprises, etc. Article 8 If there are special requirements for storage, it must be indicated on the label. Article 9 The validity period of veterinary drugs shall be marked in chronological order. The year is represented by four digits and the month by two digits, such as "valid until September 2002" or "valid until September 2002". Chapter III Basic Requirements for Instructions for Veterinary Drugs Article 10 The instructions for single, compound and Chinese and Western compound preparations of veterinary chemicals and antibiotic products must indicate the following contents: veterinary logo, name of veterinary drug, main components, properties, pharmacological effects, indications (or functional indications), usage and dosage, adverse reactions, precautions, withdrawal period, treatment measures, expiration date and contents of external pesticides and other discarded packaging that are toxic and harmful to human body or environment. Article 11 The description of Chinese veterinary drugs must indicate the following contents: animal identification, veterinary drug name, main components, properties, functional indications, usage and dosage, adverse reactions, precautions, expiration date, specifications, storage, approval number, information of production enterprises, etc. Article 12 The instructions for veterinary biological products must indicate the following contents: veterinary identification, veterinary drug name, main components and content (type of live vaccine, strain and minimum viable count or virus titer), characteristics, inoculation target, usage and dosage (dilution method must be indicated for freeze-dried vaccine), precautions (including adverse reactions and first aid measures), expiration date, specifications (capacity and first dose), packaging, storage and disposal measures for discarded packaging. Chapter IV Administration of Veterinary Drug Labels and Instructions Article 13 Veterinary drug labels and instructions must be examined and approved by the Ministry of Agriculture or the provincial animal husbandry and veterinary administrative department in accordance with the examination and approval authority of veterinary drugs. When the contents are changed, the examination and approval procedures shall be performed according to the original declaration procedures. Fourteenth veterinary drug labels and instructions must be printed in accordance with the unified requirements of these Provisions, and any unauthorized content shall not be added to its words and patterns without authorization. Fifteenth veterinary drug labels and instructions must be true and accurate, and shall not be false or exaggerated, and shall not be printed with any words and logos with propaganda and advertising colors. Sixteenth veterinary drug labels and instructions shall not exceed or delete the prescribed items; No unauthorized patents, veterinary drug GMP, trademarks and other marks may be printed. Seventeenth veterinary drug labels and instructions must be in Chinese, and use the current standard Chinese characters published by the State Language Committee. If necessary, there can be foreign language control. Eighteenth according to the needs, veterinary drug labels can use bar codes; Approved patented products can be marked with patent mark and patent number, and indicate the type of patent license; The registered trademark shall be printed on the upper left corner or upper right corner of the label and the description; To obtain a veterinary drug GMP certificate, the veterinary drug GMP mark must be used correctly in accordance with the relevant provisions on the use of veterinary drug GMP marks. Article 19 The handwriting of veterinary drug labels and instructions must be clear and easy to read, and the marks for veterinary drugs and drugs for external use should be clear and eye-catching, and there should be no phenomena such as printing falling off or weak pasting, and no modification or supplement can be made by pasting or cutting. Article 20 The descriptions of product functions and uses in veterinary drug labels and instructions shall not violate the provisions of statutory veterinary drug standards, and shall not include contents that expand the efficacy and scope of application; Its usage and dosage, withdrawal period, validity period and other items must meet the statutory veterinary drug standards, and use normative terms that meet the requirements of the national veterinary drug standards. Twenty-first veterinary drug labels and instructions must identify the generic name of veterinary drugs, but also can identify the commodity name. Commodity names shall not be associated with generic names, and there should be a certain gap with branches. The proportion of words used in generic names and commodity names shall not be less than 1: 2 (referring to the area), and shall not be less than the words used in registered trademarks.