COUGH AND CHEST CONGESTION

NDC 79481-7500 · Meijer, Inc.

Generic namedextromethorphan hydrobromide, guaifenesin

Dosage formSOLUTION

RouteORAL

Active ingredient(s)DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN

Strength10; 200 mg/15mL; mg/15mL

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

79481-7500-4 — 355 mL in 1 BOTTLE (79481-7500-4)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

79481-5330 — Dextromethorphan HBr, Guaifenesin, 79481-6101 — Dextromethorphan Hydrobromide, Doxylamine succinate, 79481-6170 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 79481-6171 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 79481-6172 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 79481-6300 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, 79481-6921 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 79481-7250 — Acetaminophen, Guaifenesin, Phenylephrine HCl, 79481-7430 — Guaifenesin, 79481-7470 — Dextromethorphan HBr and Guaifenesin, 79481-8301 — acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, 79481-8999 — acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, phenylephrine hydrochloride, 79903-042 — Benzocaine, 79903-065 — dextromethorphan hydrobromide, guaifenesin, 79903-095 — dextromethorphan hydrobromide, guaifenesin, 79903-119 — Acetaminophen, Dextromethorphan HBr, Triprolidine HCl, 79903-122 — acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, phenylephrine hydrochloride, 79903-123 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, 79903-124 — Guaifenesin, 79903-125 — guaifenesin and pseudoephedrine 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.

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