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Mucus Relief DM

NDC 55319-741 · Family Dollar (FAMILY WELLNESS)

Generic nameGuaifenesin, Dextromethorphan HBr
Dosage formTABLET, EXTENDED RELEASE
RouteORAL
Active ingredient(s)DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN
Strength60; 1200 mg/1; mg/1
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 categoryANDA

Packages

55319-741-14 — 14 BLISTER PACK in 1 CARTON (55319-741-14) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

55319-628 — ACETAMINOPHEN,DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL, 55319-641 — Acetaminophen Dextromethorphan HBr Doxylamine Succinate Phenylephrine HCI, 55319-646 — Acetaminophen Dextromethorphan HBr Phenylephrine HCl, 55319-689 — Chlorpheniramine maleate, Dextromethorphan HBr, 55319-692 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 55319-705 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 55319-731 — Dextromethorphan HBr, Guaifenesin, 55319-733 — Guaifenesin, 55319-734 — Guaifenesin, Dextromethorphan HBr, 55319-740 — Dextromethorphan HBr, Guaifenesin, 55319-754 — chlorpheniramine maleate, dextrometrorphan HBr, 55319-815 — Acetaminophen, Guaifenesin, Phenylephrine HCl, 55319-890 — Dextromethorphan Hydrobromide / Guaifenesin, 55319-891 — Guaifenesin, 55319-924 — Dextromethorphan HBr, Guaifenesin, 55319-926 — Acetaminophen, Dextromethorphan Hydrobromide and Doxylamine succinate, 55319-933 — ACETAMINOPHEN, DEXTROMETHORPHAN, PHENYLEPHRINE HCL, 55319-934 — ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HCL, 55319-954 — Acetaminophen Dextromethorphan HBr, 55319-960 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, +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