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Nighttime Cough-Kids

NDC 69676-0088 · Genexa

Generic nameChlorpheniramine maleate, Dextromethorphan HBr
Dosage formSOLUTION
RouteORAL
Active ingredient(s)DEXTROMETHORPHAN HYDROBROMIDE, CHLORPHENIRAMINE MALEATE
Strength2; 15 mg/10mL; mg/10mL
Pharmacologic classHistamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], 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

69676-0088-9 — 1 BOTTLE in 1 CARTON (69676-0088-9) / 118 mL in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

69423-999 — Dextromethorphan Hydrobromide, Doxylamine succinate and Phenylephrine Hydrochloride, 69452-478 — BROMPHENIRAMINE MALEATE, PSEUDOEPHEDRINE HYDROCHLORIDE, and DEXTROMETHORPHAN HYDROBROMIDE, 69517-155 — Acetaminophen, Phenylephrine Hydrochloride, Dextromethorphan Hydrobromide, 69517-160 — Acetaminophen, Phenylephrine, Dextromethorphan, 69517-161 — Acetaminophen, Doxylamine Succinate, Dextromethorphan HBr, 69536-315 — BROMPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, 69618-072 — Dextromethorphan HBr, Guaifenesin, 69676-0037 — Dextromethorphan HBr, Guaifenesin, 69676-0070 — Dextromethorphan HBr, Guaifenesin, 69676-0077 — Dextromethorphan HBr, Guaifenesin, 69676-0093 — Acetaminophen, Dextromethorphan HBr, 69676-0096 — Acetaminophen, Dextromethorphan HBr, 69729-003 — Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate, 69729-008 — Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride, 69729-020 — DEXTROMETHORPHAN HYDROBROMIDE and GUAIFENESIN, 69729-035 — DEXTROMETHORPHAN HYDROBROMIDE and GUAIFENESIN, 69729-036 — DEXTROMETHORPHAN HYDROBROMIDE and GUAIFENESIN, 69729-040 — DEXTROMETHORPHAN HYDROBROMIDE and GUAIFENESIN, 69729-041 — Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate, 69729-051 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, +2124 more

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