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daytime cold and flu

NDC 51316-350 · CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED

Generic nameacetaminophen, dextromethorphan Hbr, Phenylephrine HCl
Dosage formSOLUTION
RouteORAL
Active ingredient(s)ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE
Strength325; 10; 5 mg/15mL; mg/15mL; mg/15mL
Pharmacologic classAdrenergic alpha1-Agonists [MoA], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA], alpha-1 Adrenergic Agonist [EPC]
Marketing categoryOTC MONOGRAPH DRUG

Packages

51316-350-34 — 1 BOTTLE in 1 CARTON (51316-350-34) / 237 mL in 1 BOTTLE

51316-350-40 — 1 BOTTLE in 1 CARTON (51316-350-40) / 355 mL in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

51316-293 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, 51316-303 — Acetaminophen, 51316-304 — Dextromethorphan HBr, Guaifenesin, 51316-305 — Dextromethorphan HBr, Guaifenesin, 51316-310 — Dextromethorphan HBr, Guaifenesin, 51316-323 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride, 51316-324 — Acetaminophen, 51316-342 — Acetaminophen 500mg, 51316-343 — Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, 51316-344 — Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, 51316-354 — Acetaminophen, 51316-389 — Dextromethorphan HBr, Guaifenesin, 51316-390 — Acetaminophen, Caffeine, Pyrilamine maleate, 51316-401 — Acetaminophen and Ibuprofen, 51316-415 — Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, Phenylephrine HCl, 51316-421 — Acetaminophen, Dextromethorphan HBr, 51316-429 — dextromethorphan polistirex, 51316-430 — Dextromethorphan HBr, Doxylamine Succinate, 51316-431 — Dextromethorphan HBr, Doxylamine Succinate, 51316-444 — Acetaminophen, +4867 more

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