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Mucus DM

NDC 11822-5050 · Rite Aid Corporation

Generic nameDextromethorphan Hydrobromide Guaifenesin
Dosage formLIQUID
RouteORAL
Active ingredient(s)DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN
Strength20; 400 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

11822-5050-6 — 177 mL in 1 BOTTLE, PLASTIC (11822-5050-6)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

11822-2219 — dextromethorphan hydrobromide, guaifenesin, 11822-3120 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, 11822-3252 — Guaifenesin, 11822-3318 — Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate, 11822-3335 — Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, 11822-3391 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 11822-3392 — Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, 11822-4099 — acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, phenylephrine hydrochloride, 11822-4260 — Guaifenesin, 11822-5031 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 11822-5160 — Acetaminophen, Guaifenesin, Phenylephrine HCl, 11822-5462 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 11822-5832 — Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate, 11822-6005 — Dextromethorphan Hydrobromide, Doxylamine Succinate, 11822-6179 — ACETAMINOPHEN, DEXTROMETHORPHAN HBr, GUAIFENESIN, PHENYLEPHRINE HCl, 11822-7340 — Guaifenesin, Dextromethorphan HBr, 11822-7380 — Acetaminophen, Chlorpheniramine maleate, Dextromethorphan HBr, 11822-7399 — Guaifenesin and Pseudoephedrine HCL, 11822-9996 — guaifenesin and dextromethorphan hydrobromide, 12539-555 — Guaifenesin, Dextromethorphan HBr, +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