Cold, Cough, Allergy, Bronchodilator, and Antiasthmatic Drug Products for Over-The-Counter Human Use; Amendment of Final Monograph for OTC Antitussive Drug Products; Correction

Resumen

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.