药品标签是药物管理和使用的重要依据.笔者在实际工作中,发现药品标签存在着一些与法规不相符的问题.1 标签内容过于简单《药品管理法》明确规定:标签或说明书必须注明药品的品名、规格、生产企业、批准文号、产品批号、主要成分、适应证、用法、用量、禁忌、不良反应和注意事项.然而,不少生产厂家的药品标签内容极为 Drug labeling is an important basis for the management and use of drugs.In the actual work, the author found that there are some inconsistencies in the labeling of drugs.1 The content of the label is too simple The Drug Administration Law clearly stipulates that the label or instruction must specify the drugs The name, specifications, manufacturer, approval number, product lot number, main components, indications, usage, dosage, contraindications, adverse reactions and precautions.However, many manufacturers of drug labels content is extremely