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Meijer Mucus Relief DM

NDC 41250-748 · MEIJER, INC.

Generic nameDextromethorphan HBr and Guaifenesin
Dosage formSOLUTION
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

41250-748-06 — 180 mL in 1 BOTTLE (41250-748-06)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

41250-547 — Guaifenesin, Pseudoephedrine HCl, 41250-574 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 41250-603 — acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl, 41250-638 — Acetaminophen, Chlorpheniramine maleate, Dextromethorphan HBr, 41250-643 — acetaminophen, dextromethorphan HBr, guaifenesin, phenylephrine HCl, 41250-654 — guaifenesin, 41250-656 — acetaminophen, dextromethorphan Hbr, Phenylephrine HCl, 41250-663 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 41250-684 — Guaifenesin, 41250-713 — Guaifenesin, 41250-758 — dextromethorphan hydrobromide, doxylamine succinate, 41250-763 — Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, Phenylephrine HCl, 41250-776 — dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride, 41250-811 — Acetaminophen, dextromethorphan HBr, doxylamine succinate, phenylephrine HCl, 41250-812 — dextromethorphan HBr, guaifenesin, 41250-869 — Acetaminophen, Dextromethorphan HBr, Triprolidine HCl, 41250-877 — Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, Phenylephrine HCl, 41250-899 — Dextromethorphan polistirex, 41250-958 — dextromethorphan polistirex, 41250-979 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE 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.