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Cold and Flu

NDC 51316-963 · CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED

Generic nameAcetaminophen, Dextromethorphan HBr, Triprolidine HCl
Dosage formSOLUTION
RouteORAL
Active ingredient(s)ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, TRIPROLIDINE HYDROCHLORIDE
Strength650; 20; 2.5 mg/20mL; mg/20mL; mg/20mL
Pharmacologic classSigma-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

51316-963-45 — 177 mL in 1 BOTTLE, PLASTIC (51316-963-45)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

51316-877 — Dextromethorphan hydrobromide, 51316-884 — Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine succinate, 51316-896 — Acetaminophen Dextromethorphan HBr Phenylephrine HCl, 51316-897 — Acetaminophen, Dextromethorphan HBr, 51316-921 — Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine succinate, 51316-927 — Acetaminophen, Guaifenesin, Phenylephrine HCl, 51316-940 — Acetaminophen, Guaifenesin, 51316-943 — dextromethorphan polistirex, 51316-945 — Acetaminophen, Chlorpheniramine Maleate and Dextromethophan HBr, 51316-955 — Acetaminophen and Ibuprofen, 51316-969 — Acetaminophen 650mg, 51352-189 — Acetaminophen, Guaifenesin, Pentoxyverine citrate, Phenylpehrine Hydcrochloride, Chlorpheniramine Maleate, Caffeine Anhydrous, 51376-130 — Acetaminophen, 51407-556 — Butalbital, Acetaminophen and Caffeine, 51467-005 — Acetaminophen, Chlorpheniramine maleate, Phenylephrine hydrochloride, 51467-006 — ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, PHENYLEPHRINE HYDROCHLORIDE, 51467-007 — ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE, 51467-008 — ACETAMINOPHEN, PHENYLEPHRINE HYDROCHLORIDE, 51467-010 — Acetaminophen, Chlorpheniramine maleate, Phenylephrine hydrochloride, 51467-011 — Acetaminophen, Chlorpheniramine maleate, Phenylephrine hydrochloride, +4426 more

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