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WINCO

NDC 67091-457 · WINCO FOODS, LLC

Generic nameAcetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl
Dosage formSOLUTION
RouteORAL
Active ingredient(s)ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE
Strength650; 20; 400; 10 mg/20mL; mg/20mL; mg/20mL; mg/20mL
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

67091-457-06 — 180 mL in 1 BOTTLE, PLASTIC (67091-457-06)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

67091-345 — Guaifenesin, Dextromethorphan HBr, 67091-349 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 67091-355 — Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride, 67091-370 — Guaifenesin, 67091-394 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCL, 67091-395 — ACETAMINOPHEN DEXTROMETHORPHAN HYDROBROMIDE DOXYLAMINE SUCCINATE, 67091-401 — Acetaminophen, 67091-403 — Guaifenesin, 67091-404 — Guaifenesin, 67091-426 — Acetaminophen, Chlorpheniramine maleate, 67091-469 — Dextromethorphan HBr, Guaifenesin, 67091-470 — Dextromethorphan HBr Guaifenesin Phenylephrine HCl, 67091-471 — Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride, 67091-691 — Dextromethorphan HBr Guaifenesin Phenylephrine HCl, 67172-015 — Menthol and Benzocaine and Dextromethorphan Hydrobromide, 67172-016 — Menthol and Benzocaine and Dextromethorphan Hydrobromide, 67172-150 — acetaminophen and diphenhydramine hydrochloride, 67172-503 — Phenylephrine hydrochloride and Glycerin, 67296-0836 — Oxycodone and Acetaminophen, 67296-1467 — Guaifenesin, +5267 more

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