美国FDA 指导原则 根据《膳食补充剂和非处方药消费者保护法》的要求，在未经批准的情况下销售的非处方药产品的标签问答 英文原版.pdfVIP

Guidance for Industry Labeling of Nonprescription Human Drug Products Marketed Without an Approved Application as Required by the Dietary Supplement and Nonprescription Drug Consumer Protection Act: Questions and Answers U.S. Department of Health and Human Services Food and Drug Administration Center for Drug Evaluation and Research (CDER) September 2009 OTC OMB Control Number 0910-0340 Cu