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cold and flu

NDC 42507-001 · HyVee Inc

Generic nameAcetaminophen, Dextromethorphan HBr, Doxylamine succinate
Dosage formSOLUTION
RouteORAL
Active ingredient(s)ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE
Strength650; 30; 12.5 mg/30mL; mg/30mL; mg/30mL
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

42507-001-40 — 355 mL in 1 BOTTLE (42507-001-40)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

41520-931 — Dextromethorphan HBr, Guaifenesin, 41520-956 — Acetaminophen, Diphenhydramine HCl, 41520-958 — dextromethorphan polistirex, 41520-984 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, 41520-985 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, 42192-607 — Brompheniramine Maleate, Pseudoephedrine Hydrochloride, and Dextromethorphan Hydrobromide, 42192-630 — Brompheniramine Maleate, Pseudoephedrine Hydrochloride, and Dextromethorphan Hydrobromide, 42291-181 — Butalbital, Acetaminophen, and Caffeine, 42364-0011 — acetaminophen, aspirin, and caffeine, 42364-2208 — acetaminophen, aspirin, and caffeine, 42507-020 — Acetaminophen, dextromethorphan HBr, doxylamine succinate, phenylephrine HCl, 42507-033 — Doxylamine succinate, 42507-056 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 42507-095 — Acetaminophen and Diphenhydramine Hydrochloride, 42507-103 — Acetaminophen, 42507-148 — Acetaminophen, 42507-163 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 42507-170 — Acetaminophen, 42507-173 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 42507-205 — Acetaminophen, +4482 more

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