Fed Regist. 1999 Sep 14;64(177):49652-5.
The Food and Drug Administration (FDA) is amending the regulations for internal analgesic, antipyretic, and antirheumatic drug products for over-the-counter (OTC) use to correct inadvertent errors and to clarify the labeling for over-the-counter drug products written for health professionals.
美国食品药品监督管理局(FDA)正在修订用于非处方(OTC)的内服止痛、退热和抗风湿药品的法规,以纠正无意出现的错误,并阐明为医疗专业人员编写的非处方药品标签。