Cough and Congestion DM

NDC 63941-817 · Best Choice (Valu Merchandisers Company)

Generic nameDextromethorphan Hydrobromide, Guaifenesin

Dosage formLIQUID

RouteORAL

Active ingredient(s)DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN

Strength20; 200 mg/10mL; mg/10mL

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

63941-817-04 — 1 BOTTLE, PLASTIC in 1 BOX (63941-817-04) / 118 mL in 1 BOTTLE, PLASTIC

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

63941-473 — Acetaminophen, Chlorpheniramine maleate, Dextromethorphan HBr, Phenylephrine HCl, 63941-497 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 63941-498 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 63941-499 — Dextromethorphan HBr, Doxylamine Succinate, 63941-509 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 63941-517 — DEXTROMETHORPHAN HBr, GUAIFENESIN, PHENYLEPHRINE HCL, 63941-518 — DEXTROMETHORPHAN HBr, GUAIFENESIN, PHENYLEPHRINE HCL, 63941-731 — Guaifenesin, 63941-733 — Guaifenesin, Dextromethorphan HBr, 63941-734 — Guaifenesin, Dextromethorphan HBr, 63941-823 — Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 63941-985 — Dextromethorphan Hydrobromide / Guaifenesin, 63941-986 — Guaifenesin/phenylephrine, 63941-987 — Guaifenesin, 63941-989 — Chlorpheniramine maleate, Dextromethorphan HBr, 63981-812 — dextromethorphan HBr, guaifenesin, 64597-301 — dextromethorphan hydrobromide and quinidine sulfate, 65131-011 — ACETAMINOPHEN-CHLORPHENIRAMINE MALEATE-DEXTROMETHORPHAN HBr-GUAIFENESIN-PHENYLEPHRINE HCl, 65131-035 — DEXTROMETHORPHAN HBR-PYRILAMINE MALEATE, 65131-054 — ACETAMINOPHEN-PHENYLEPHRINE HCl-GUAIFENESIN, +2508 more

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

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels