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Robitussin Peak Cold Multi-Symptom Cold

NDC 0031-8742 · Haleon US Holdings LLC

Generic namedextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride
Dosage formLIQUID
RouteORAL
Active ingredient(s)DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE
Strength10; 100; 5 mg/5mL; mg/5mL; mg/5mL
Pharmacologic classAdrenergic alpha1-Agonists [MoA], Decreased 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], alpha-1 Adrenergic Agonist [EPC]
Marketing categoryOTC MONOGRAPH DRUG

Packages

0031-8742-14 — 1 BOTTLE in 1 CARTON (0031-8742-14) / 118 mL in 1 BOTTLE

0031-8742-20 — 1 BOTTLE in 1 CARTON (0031-8742-20) / 237 mL in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0031-8693 — chlorpheniramine maleate, dextrometrorphan HBr, 0031-8694 — dextromethorphan hydrobromide, 0031-8702 — dextromethorphan hydrobromide and guaifenesin, 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, 0031-8743 — dextromethorphan hydrobromide, 0031-8744 — acetaminophen, dextromethorphan hydrobromide, and doxylamine succinate, 0031-8750 — acetaminophen, dextromethorphan hydrobromide, 0031-8751 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, 0031-8752 — 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, +3082 more

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