检查内容包括：1、对于未经药品监督管理部门批准生产的、整件包装无出厂检

The inspection contents include: 1. For products that have not been approved by the drug regulatory department, the whole package has no factory inspection certificate, the contents of the label instructions are not within the scope of approval, and those purchased from illegal enterprises have obvious appearance and qualified products. Drugs with different internal and external packaging with obvious damage or loose sealing shall be regarded as unqualified, rejected, and reported for processing; 2. When receiving, the packaging, labels, instructions and certificates or documents of relevant requirements shall be checked one by one. 3. Check the outer packaging, such as whether the packaging box is firm and dry, whether the seals and seals are damaged, whether the packaging box is leaking, stained or damaged, and the product name, specification, product batch number, and production date should be clearly marked on the outer packaging. , expiration date, storage, packaging, approval number and transportation precautions or other markings, such as non-prescription drug labels. 4. The inner packaging should check whether the container is clean, dry and undamaged; the seal is tight; the packaging is clearly printed and the bottle label is firmly pasted. 5. Inspection of packaging labels and instructions: the generic name, ingredients, specifications, manufacturer, approval number, product batch number, production date, expiration date, indications or functions, usage and dosage, contraindications, Adverse reactions and precautions. 6. There should be a product certificate in each whole package of the product.

The inspection contents include: 1. The drugs produced without the approval of the drug regulatory department, the whole package without factory inspection certificate, the contents of the label instructions are not within the scope of approval, the drugs purchased from illegal enterprises, the properties and appearance are significantly different from the qualified products, the inner and outer packages are obviously damaged or the sealing is not tight are regarded as unqualified, rejected and reported for treatment; 2. Upon receipt, the packaging, labels, instructions and certificates or documents of relevant requirements of drugs shall be checked one by one. 3. External packaging inspection, such as whether the packaging box is firm and dry, whether the seal and seal are damaged, and whether the packaging box is leaking, stained and damaged. The product name, specification, product batch number, production date, expiration date, storage, packaging, approval number, transportation precautions or other marks, such as the identification of over-the-counter drugs, shall be clearly indicated on the external packaging. 4. The inner packaging shall check whether the container is clean, dry and free from damage; Tight sealing; The packaging printing is clear and the bottle label is pasted firmly. 5. Inspection of packaging labels and instructions: the general name, composition, specification, manufacturer, approval number, product batch number, production date, expiration date, indication or function, usage and dosage, contraindications, adverse reactions and precautions of the drug must be indicated on the label or instructions. 6. Each complete package of the product shall have a product certificate.

The inspection contents include: 1. Drugs that are produced without the approval of the drug supervision and administration department, have no factory inspection certificate for the whole package, the contents of the label instructions are not within the approved scope, are purchased from illegal enterprises, have obvious differences between the appearance and the qualified products, and the internal and external packages are obviously damaged or the seals are not tight, which are regarded as unqualified, rejected and reported for processing; 2. Check the package, label, instructions and relevant certificates or documents of drugs one by one when receiving them. 3. Check the outer packaging, such as whether the packing box is firm and dry, whether the seal and seal are damaged, whether the packing box is leaking, defaced and damaged, and clearly indicate the name, specification, product batch number, production date, expiration date, storage, packaging, approval number, precautions for transportation or other marks on the outer packaging, such as over-the-counter drug identification, etc. 4. The inner packaging should check whether the container is clean, dry and free of damage; Seal tightly; Packaging printing is clear, bottle label is firmly pasted. 5. Inspection of packaging labels and instructions: the 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 and dosage, contraindications, adverse reactions and matters needing attention. 6. Every whole package of the product should have the product certificate.