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DEXTROMETHORPHAN HYDROBROMIDE and GUAIFENESIN

NDC 69729-040 · OPMX LLC

Generic nameDEXTROMETHORPHAN HYDROBROMIDE and GUAIFENESIN
Dosage formSYRUP
RouteORAL
Active ingredient(s)DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN
Strength20; 300 mg/5mL; mg/5mL
Pharmacologic classDecreased 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]
Marketing categoryOTC MONOGRAPH DRUG

Packages

69729-040-04 — 118 mL in 1 BOTTLE (69729-040-04)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

69676-0070 — Dextromethorphan HBr, Guaifenesin, 69676-0077 — Dextromethorphan HBr, Guaifenesin, 69676-0088 — Chlorpheniramine maleate, Dextromethorphan HBr, 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, 69729-041 — Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate, 69729-051 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 69729-054 — Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate, 69729-056 — Acetaminophen, Dextromethorphan Hydrobromide, 69729-057 — Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate, 69729-062 — DEXTROMETHORPHAN HYDROBROMIDE and GUAIFENESIN, 69729-069 — DEXTROMETHORPHAN HYDROBROMIDE and GUAIFENESIN, 69729-070 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 69729-108 — DEXTROMETHORPHAN HYDROBROMIDE and GUAIFENESIN, 69729-120 — Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride, +2508 more

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