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Cold and Flu Relief

NDC 37808-864 · H E B

Generic nameAcetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride
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

37808-864-16 — 16 BLISTER PACK in 1 CARTON (37808-864-16) / 1 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

37808-730 — Guaifenesin, Dextromethorphan HBr, 37808-733 — Guaifenesin, Dextromethorphan HBr, 37808-747 — Acetaminophen, 37808-763 — Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, Phenylephrine HCl, 37808-775 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 37808-792 — Acetaminophen, 37808-795 — Acetaminophen and Diphenhydramine Hydrochloride, 37808-811 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 37808-834 — Guaifenesin, Dextromethorphan HBr, 37808-848 — Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride, 37808-945 — Acetaminophen, 37808-980 — Acetaminophen, 37808-987 — Brompheniramine maleate, Dextromethorphan HBr, Phenylephrine HCl, 37808-994 — Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride, 37835-403 — Guaifenesin, Dextromethorphan HBr, 37835-507 — Acetaminophen, 37835-512 — ACETAMINOPHEN, 37835-520 — acetaminophen, dextromethorphan hydrobromide, phenylephrine hydrochloride, 37835-522 — Acetaminophen, Doxylamine Succinate, Dextromethorphan HBr, 37835-524 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, +4867 more

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