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Cold, Cough, Allergy, Bronchodilator, and Antiasthmatic Drug Products for Over-The-Counter Human Use; Amendment of Final Monograph for OTC Antitussive Drug Products; Correction
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Zusammenfassung
The Food and Drug Administration (FDA) is correcting a final rule that appeared in the Federal Register of June 3, 1994 (59 FR 29172). The document amended the final monograph for over-the-counter (OTC) antitussive drug products to include the ingredients diphenhydramine citrate and diphenhydramine hydrochloride. The document was published with some errors. This document corrects those errors.
Originalsprache der Quelle: Federal Register — Health and Human ServicesOriginalquelle öffnen →