severe cold and flu

NDC 51316-293 · CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED

Generic nameacetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride

Dosage formSOLUTION

RouteORAL

Active ingredient(s)ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE

Strength325; 10; 200; 5 mg/15mL; mg/15mL; mg/15mL; mg/15mL

Pharmacologic classAdrenergic alpha1-Agonists [MoA], Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], 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

51316-293-40 — 355 mL in 1 BOTTLE (51316-293-40)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

51316-177 — Acetaminophen, 51316-179 — acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, phenylephrine hydrochloride, 51316-185 — ACETAMINOPHEN, 51316-188 — ACETAMINOPHEN, 51316-189 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, 51316-203 — GLYCERIN, PHENYLEPHRINE HYDROCHLORIDE, PRAMOXINE HYDROCHLORIDE, WHITE PETROLATUM, 51316-225 — GLYCERIN, LIDOCAINE, PHENYLEPHRINE HYDROCHLORIDE, WHITE PETROLATUM, 51316-228 — MINERAL, PETROLATUM, PHENYLEPHRINE HYDROCHLORIDE, 51316-263 — dextromethorphan polistirex, 51316-282 — Acetaminophen, 51316-299 — guaifenesin, 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, +5267 more

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