The labels of narcotic drugs, psychotropic drugs, toxic drugs for medical use, radioactive drugs, external drugs and over-the-counter drugs must bear the prescribed logo.

1. Article 14 of the "Regulations on the Administration of Drug Packaging, Labeling and Instructions" (Interim) stipulates that narcotic drugs, psychotropic drugs, toxic drugs for medical use, radioactive drugs and other specially managed drugs, drugs for external use, Over-the-counter drugs are packaged, bulk-packed and labeled;

Instructions must be printed with compliant signs; drugs with special storage requirements must be clearly stated on the packaging, labels and instructions.

2. Article 54 of the "Drug Administration Law": "Drug packaging must be printed or affixed with labels and instructions in accordance with regulations. The label or instructions must indicate the common name, ingredients, and ingredients of the drug. Specifications, manufacturer, approval number, product batch number, production date, expiry date, functions and indications, usage, dosage, contraindications, adverse reactions and precautions

3. "Regulations on the Management of Drug Packaging, Labeling and Instructions." 》Article 9: Drug labels are divided into inner packaging labels and outer packaging labels.

1. The content of the inner packaging labels and outer packaging labels shall not exceed the content limited by the drug instructions approved by the State Food and Drug Administration; The text expression should be consistent with the instructions.

2. The inner packaging label can include the name of the drug, indications or functions, usage and dosage, specifications, storage, production date, and production according to its size. Batch number, expiry date, production company and other labeling contents, but the name, specifications and production batch number of the drug must be marked.

3. The name, main ingredients, properties, indications or functions and indications of the drug should be indicated on the packaging label. Usage and dosage, adverse reactions, contraindications, specifications, storage, production date, production batch number, validity period, approval number, production company, etc.

4. The large package label should indicate the drug name, specifications, Storage, production date, production batch number, expiration date, approval number, production company and necessary content other than those specified in the instruction manual, including packaging quantity, transportation precautions or other marks, etc.

5.) The expiration date on the label. The specific expression form should be: Valid until × year × month

6. Due to size reasons, if the adverse reactions, contraindications, and precautions cannot be fully stated on the packaging label, "See for details." "Instruction Manual".

Extended information:

Memory tips for the management of narcotic drugs and psychotropic drugs:

1. Ma Jing Yi Seal Card: Municipal Health Administration The Ministry of Health approves the issuance, reports it to the Provincial Ministry of Health for record, and sends a copy to the municipal pharmacy and the public security agency.

2. Seal card application conditions: Have a diagnosis and treatment subject, have full-time pharmacy technicians, and have prescription qualifications. Physicians, have safe storage facilities and management systems.

3. Validity period of seal card: 3 years and 3 months. 4. Special account book: 5 years after expiration.

5. Comparison of wholesale enterprises of narcotic drugs and psychotropic drugs: "Narcotics and Class I psychotropic drugs have two levels of national approval and regional approval; national approval and State Food and Drug Administration approval qualifications can be purchased from designated production enterprises; Mainly supplied to each province for regional approval, for qualified hospitals to be approved by provincial drug administration;

For regional approval, provincial drug administration approval is required, purchased from the national batch, and purchased from designated production enterprises require provincial drug administration approval; mainly for provincial qualifications Hospitals, supply to cross-provincial hospitals require approval from the National Food and Drug Administration, and regional batch transfers require the Provincial Food and Drug Administration."

6. Mailing certificates and transportation certificates are both issued by the Provincial Food and Drug Administration.

7. If the hospital urgently needs anesthesia to rescue patients, report it to the municipal drug administration and the Ministry of Health for record.

8. The county-level drug administration shall supervise the destruction of anesthetic drugs.

9. Retail of Category II psychotropic drugs: Retail chain retail of Category II psychotropic drugs has been approved by the municipal drug administration. Physician prescriptions are kept for 2 years. Overdosage is prohibited for minors.

10. The transportation certificate of hemp essence is valid for one year.

Chinese Government Website—State Food and Drug Administration Order