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NIGHTTIME COUGH DM

NDC 51316-791 · CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED

Generic nameDextromethorphan Hydrobromide, Doxylamine Succinate
Dosage formSOLUTION
RouteORAL
Active ingredient(s)DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE
Strength30; 12.5 mg/20mL; mg/20mL
Pharmacologic classAntihistamine [EPC], Histamine Receptor Antagonists [MoA], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA]
Marketing categoryOTC MONOGRAPH DRUG

Packages

51316-791-26 — 1 BOTTLE in 1 CARTON (51316-791-26) / 118 mL in 1 BOTTLE (51316-791-00)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

51316-692 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 51316-727 — ACETAMINOHPEN, DEXTROMETHORPHAN HBr, GUAIFENESIN PHENYLEPHRINE HCL, 51316-731 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, 51316-738 — Acetaminophen, Chlorpheniramine maleate, Dextromethorphan HBr, 51316-740 — Dextromethorphan HBr, Guaifenesin, 51316-744 — dextromethorphan hydrobromide and guaifenesin, 51316-745 — chlorpheniramine maleate, dextrometrorphan HBr, 51316-752 — Chlorpheniramine maleate and Dextromethorphan Hydrobromide, 51316-775 — Dextromethorphan HBr, Guaifenesin, 51316-778 — Dextromethorphan Hydrobromide, 51316-803 — Acetaminophen, Dextromethorphan HBr, 51316-808 — Dextromethorphan HBr, Guaifenesin, 51316-815 — Dextromethorphan HBr, guaifenesin, Phenylephrine HCl, 51316-826 — Dextromethorphan Hydrobromide, Guaifenesin, 51316-830 — Dextromethorphan hydrobromide, Guaifenesin, 51316-858 — dextromethorphan hydrobromide, guaifenesin, 51316-877 — Dextromethorphan hydrobromide, 51316-884 — Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine succinate, 51316-896 — Acetaminophen Dextromethorphan HBr Phenylephrine HCl, 51316-897 — Acetaminophen, Dextromethorphan HBr, +2034 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.