This is the Management Measures for Veterinary Drug Labels and Instructions. The following are the precautions for labels. Chapter 2 Basic Requirements for Veterinary Drug Labels. Article 4 Veterinary drug products (except raw materials) must use both inner packaging labels and outer packaging labels. . Article 5 The inner packaging label must indicate the veterinary logo, name of the veterinary drug, indications (or functions and indications), content/packaging specifications, approval number or "Import Veterinary Drug Registration License" number, production date, production batch number, Validity period, production company information, etc. If ampoules, vials and other injection or oral products cannot indicate all the above contents due to packaging size restrictions, the items may be appropriately reduced, but at least the name of the veterinary drug, content specification, and production batch number must be indicated. Article 6 The outer packaging label must indicate the veterinary logo, name of the veterinary drug, main ingredients, indications (or functions and indications), usage and dosage, content/packaging specifications, approval number or "Import Veterinary Drug Registration License" number , production date, production batch number, validity period, withdrawal period, storage, packaging quantity, production enterprise information, etc. Article 7 The label of veterinary raw materials must indicate the name of the veterinary drug, packaging specifications, production batch number, production date, validity period, storage, approval number, transportation precautions or other marks, production enterprise information, etc. Article 8 Special requirements for storage must be clearly stated 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 is represented by two digits, such as "valid until September 2002", or "valid until September 2002." Chapter 4 Management of Veterinary Drug Labels and Instructions Article 13 Veterinary drug labels and instructions must be reviewed and approved by the Ministry of Agriculture or the provincial animal husbandry and veterinary administrative department in accordance with the veterinary drug approval authority before use. When the content is changed, the approval procedures must be carried out according to the original application procedures. Article 14 Veterinary drug labels and instructions must be printed in accordance with the unified requirements of these regulations, and any unapproved content must not be added to their text and graphics. Article 15 The contents of veterinary drug labels and instructions must be true and accurate, and must not be false or exaggerated, nor may they contain any words or logos with propaganda or advertising colors. Article 16 The contents of veterinary drug labels and instructions shall not exceed or delete the specified items; they shall not be printed with unapproved patents, veterinary drug GMP, trademarks and other marks. Article 17 The text used in labels and instructions for veterinary drugs must be in Chinese, and use the current standardized Chinese characters announced by the National Language and Writing Committee. Foreign language comparisons are available as needed. Article 18 As needed, barcodes can be used on veterinary drug labels; approved patented products can be marked with patent marks and patent numbers, and indicate the type of patent license; registered trademarks should be printed in the upper left or upper right corner of labels and instructions ; Those who have obtained the veterinary drug GMP certificate must correctly use the veterinary drug GMP logo in accordance with the relevant regulations on the use of veterinary drug GMP logos. Article 19 The handwriting on veterinary drug labels and instructions must be clear and legible. Veterinary labels and external drug labels must be clear and eye-catching. There must be no signs of falling off or weak pasting, and modifications or additions must not be made by pasting or cutting. . Article 20 The expressions of product functions and usage items in the labels and instructions of veterinary drugs shall not violate the provisions of legal veterinary drug standards, and shall not contain content that expands the efficacy and scope of application; their usage and dosage, drug withdrawal period, validity period and other items must It is consistent with the statutory veterinary drug standards and uses normative terms that comply with the requirements of the national veterinary drug standards. Article 21 The generic name of the veterinary drug must be marked on the labels and instructions of the veterinary drug, and the trade name may be marked at the same time. The product name must not be written in conjunction with the common name, and there should be a certain space between the two and separate lines. The ratio of the common name to the trade name shall not be less than 1:2 (referring to the area), and shall not be smaller than that of the registered trademark. Article 22 The packaging of the smallest sales unit of veterinary drugs must be printed or affixed with a label that complies with the provisions of the outer packaging label and must be accompanied by instructions.

The outer packaging box of veterinary drugs must have an outer packaging label printed or affixed to it. Article 23 Anyone who violates the provisions of these Measures shall be punished in accordance with the relevant provisions of the "Regulations on the Administration of Veterinary Drugs". As far as label style is concerned: I am not an expert. I don’t know much about it. If the poster is a professional, you can check out the forum /show.asp?id=2131643. There are some good design solutions on it. Finally, I wish the author a speedy and prosperous career.