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Mucus Relief DM

NDC 70000-0565 · Cardinal Health (Leader) 70000

FDA lists marketing as ended on 2026-08-28.
Generic nameDextromethorphan HBr, 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

70000-0565-1 — 177 mL in 1 BOTTLE, PLASTIC (70000-0565-1)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70000-0195 — dextromethorphan polistirex, 70000-0278 — Dextromethorphan HBr and Guaifenesin, 70000-0302 — dextromethorphan polistirex, 70000-0324 — Chlorpheniramine maleate, Dextromethorphan HBr, 70000-0464 — Guaifenesin, Dextromethorphan HBr, 70000-0479 — Guaifenesin, 70000-0491 — Guaifenesin, Dextromethorphan HBr, 70000-0515 — ACETAMINOHPEN, DEXTROMETHORPHAN HBr, PHENYLEPHRINE HCL, 70000-0516 — ACETAMINOPHEN DEXTROMETHORPHAN HYDROBROMIDE DOXYLAMINE SUCCINATE, 70000-0525 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 70000-0596 — dextromethorphan hydrobromide, guaifenesin, 70000-0623 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride, 70000-0628 — Dextromethorphan HBr, Guaifenesin, 70000-0629 — Dextromethorphan HBr, guaifenesin, Phenylephrine HCl, 70000-0630 — Dextromethorphan HBr, Guaifenesin, 70000-0636 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, 70000-0652 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 70000-0670 — Dextromethorphan HBr, Guaifenesin, 70000-0673 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 70000-0696 — 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.