adult tussin dm

NDC 69842-513 · CVS Pharmacy

Generic namedextromethorphan hydrobromide, guaifenesin

Dosage formSOLUTION

RouteORAL

Active ingredient(s)DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN

Strength20; 200 mg/20mL; mg/20mL

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

69842-513-26 — 1 BOTTLE in 1 CARTON (69842-513-26) / 118 mL in 1 BOTTLE

69842-513-34 — 1 BOTTLE in 1 CARTON (69842-513-34) / 237 mL in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

69842-059 — Guaifenesin and Dextromethorphan HBr, 69842-086 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 69842-095 — Guaifenesin 600 mg and Pseudoephedrine HCl 60 mg, 69842-211 — Guaifenesin and Pseudoephedrine HCL, 69842-335 — Guaifenesin, 69842-377 — Benzocaine, 69842-475 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 69842-487 — Childrens Stuffy Nose and Cold, 69842-503 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 69842-505 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 69842-566 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin ,Phenylephrine HCL, 69842-570 — Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 69842-577 — DEXTROMETHORPHAN HYDROBROMIDE AND GUAIFENESIN, 69842-616 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE, 69842-634 — Dextromethorphan HBr, 69842-651 — Acetaminophen, Guaifenesin, Phenylephrine HCl, 69842-689 — Chlorpheniramine maleate, Dextromethorphan HBr, 69842-699 — Dextromethorphan HBr, Doxylamine succinate, 69842-717 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 69842-723 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, 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.