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Robitussin Maximum Strength Severe Cough Plus Sore Throat

NDC 0031-8750 · Haleon US Holdings LLC

Generic nameacetaminophen, dextromethorphan hydrobromide
Dosage formLIQUID
RouteORAL
Active ingredient(s)ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE
Strength650; 20 mg/20mL; mg/20mL
Pharmacologic classSigma-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

0031-8750-12 — 1 BOTTLE in 1 CARTON (0031-8750-12) / 118 mL in 1 BOTTLE

0031-8750-18 — 1 BOTTLE in 1 CARTON (0031-8750-18) / 237 mL in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0031-8715 — dextromethorphan hydrobromide, guaifenesin, 0031-8716 — dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride, 0031-8718 — dextromethorphan hydrobromide, doxylamine succinate, 0031-8719 — dextromethorphan hydrobromide and guaifenesin, 0031-8725 — dextromethorphan polistirex, 0031-8726 — dextromethorphan polistirex, 0031-8739 — dextromethorphan hbr, guaifenesin, 0031-8742 — dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride, 0031-8743 — dextromethorphan hydrobromide, 0031-8744 — acetaminophen, dextromethorphan hydrobromide, and doxylamine succinate, 0031-8751 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, 0031-8752 — acetaminophen, diphenhydramine hydrochloride, 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, 0031-8758 — dextromethorphan HBr, doxylamine succinate, 0031-8759 — dextromethorphan hydrobromide, guaifenesin, 0031-8760 — dextromethorphan HBr, guaifenesin, +4418 more

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