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Daytime Cold and Flu Relief

NDC 76162-065 · TopCo Associates, LLC

Generic nameDaytime Cold and Flu Relief
Dosage formCAPSULE, LIQUID FILLED
RouteORAL
Active ingredient(s)ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE
Strength325; 10; 5 mg/1; mg/1; mg/1
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

76162-065-16 — 1 BLISTER PACK in 1 CARTON (76162-065-16) / 16 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

76095-011 — Acetaminophen Chlorpheniramine Maleate Phenylepherine Hydrochloride, 76095-012 — Guaifensin, Dextromethorphan, 76117-001 — CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE, 76162-000 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride, 76162-008 — Mucus Relief DM, 76162-026 — Nite Time Cold and Flu Relief, 76162-032 — GUAIFENESIN AND DEXTROMETHORPHAN HBR, 76162-040 — Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 76162-050 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 76162-057 — Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 76162-079 — Acetaminophen, 76162-099 — brompheniramine maleate, dextromethorphan hydrobromide, 76162-142 — Acetaminophen, Aspirin, Caffeine, 76162-198 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, 76162-202 — acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, phenylephrine hydrochloride, 76162-294 — Dextromethorphan HBr, Guaifensin, 76162-483 — acetaminophen, dextromethorphan hydrobromide, 76162-500 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, 76162-501 — Acetaminophen, Ibuprofen, 76162-520 — acetaminophen, ibuprofen, +4867 more

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