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Robitussin Honey Maximum Strength Nighttime Cough DM

NDC 0031-8758 · Haleon US Holdings LLC

Generic namedextromethorphan HBr, doxylamine succinate
Dosage formSOLUTION
RouteORAL
Active ingredient(s)DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE
Strength30; 12.5 mg/20mL; mg/20mL
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

0031-8758-12 — 1 BOTTLE in 1 CARTON (0031-8758-12) / 118 mL in 1 BOTTLE

0031-8758-18 — 1 BOTTLE in 1 CARTON (0031-8758-18) / 237 mL in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0031-8742 — dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride, 0031-8743 — dextromethorphan hydrobromide, 0031-8744 — acetaminophen, dextromethorphan hydrobromide, and doxylamine succinate, 0031-8750 — acetaminophen, dextromethorphan hydrobromide, 0031-8751 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, 0031-8753 — dextromethorphan polistirex, 0031-8754 — dextromethorphan polistirex, 0031-8755 — dextromethorphan polistirex, 0031-8756 — dextromethorphan HBr, guaifenesin, 0031-8757 — dextromethorphan hydrobromide and guaifenesin, 0031-8759 — dextromethorphan hydrobromide, guaifenesin, 0031-8760 — dextromethorphan HBr, guaifenesin, 0031-8762 — dextromethorphan hbr, doxylamine succinate, 0031-8765 — Dextromethorphan Hydrobromide, Guaifenesin, 0031-8771 — acetaminophen, dextromethorphan hbr, 0031-9302 — dextromethorphan hydrobromide, 0031-9306 — dextromethorphan hydrobromide, menthol, 0031-9307 — dextromethorphan hydrobromide, menthol, 0031-9310 — dextromethorphan hydrobromide, 0031-9311 — dextromethorphan hydrobromide, doxylamine succinate, +2034 more

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