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- W2044812744 abstract "To the Editor.— The Food and Drug Administration (FDA) is in the midst of a major scientific review, by 17 extramural advisory panels, of all of the ingredients in over-the-counter (OTC) drugs. One such hard-working panel, which included myself, recently submitted its report on laxatives, antidiarrheals, antiemetics, and emetics, as published in theFederal Register.1Industry and other interested persons have 60 days in which to reply to the initial reports, following which the FDA may utilize the panel's advice to issue a final monograph defining the safe and effective ingredients of a class of products. The monograph on antacids is already in effect, and the antimicrobial panel is currently undergoing final review by the FDA. Physicians should be aware not only of the scope of this endeavor but of the opportunity to eliminate unsafe and often anachronistic compounds still sold OTC. The Laxative Panel, for example, classified as" @default.
- W2044812744 created "2016-06-24" @default.
- W2044812744 creator A5080602934 @default.
- W2044812744 date "1975-07-21" @default.
- W2044812744 modified "2023-10-16" @default.
- W2044812744 title "OTC Drug Review and Toxic Anachronisms" @default.
- W2044812744 doi "https://doi.org/10.1001/jama.1975.03260030016006" @default.
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