Relevant laws and regulations on drug labels and instructions?

Drug Administration Law Article 54 Drug packaging must be printed or labeled with instructions in accordance with regulations. Labels or instructions must indicate the generic name, ingredients, specifications, manufacturer, approval number, product batch number, production date, expiration date, indications or functional indications, usage, dosage, contraindications, adverse reactions and precautions. The labels of narcotic drugs, psychotropic drugs, toxic drugs for medical use, radioactive drugs, drugs for external use and over-the-counter drugs must be marked with prescribed marks.