Wollschlaeger Bernd
Department of Medicine and Family Medicine, University of Miami School of Medicine, Miami, Florida, USA.
Int J Toxicol. 2003 Sep-Oct;22(5):387-90. doi: 10.1177/109158180302200509.
The Dietary Supplement and Health Education Act (DSHEA) of 1994 was intended to ensure consumer access to safe dietary supplements, e.g., herbs, minerals, and vitamins. It granted the Food and Drug Administration (FDA) considerable enforcement authority to regulate dietary supplement industry. This article discusses relevant components of the DSHEA, explains the division of regulatory responsibilities between the FDA and the Federal Trade Commission (FTC), and refutes the often cited allegation that the herb and dietary supplement industry are unregulated.
1994年的《膳食补充剂健康教育法》(DSHEA)旨在确保消费者能够获得安全的膳食补充剂,例如草药、矿物质和维生素。它赋予了美国食品药品监督管理局(FDA)相当大的执法权力来监管膳食补充剂行业。本文讨论了DSHEA的相关组成部分,解释了FDA与联邦贸易委员会(FTC)之间监管职责的划分,并驳斥了经常被提及的关于草药和膳食补充剂行业缺乏监管的指控。