Mucus Relief DM

NDC 60000-057 · Ahold U.S.A., Inc,

Generic nameGuaifenesin and Dextromethorphan HBr

Dosage formTABLET, EXTENDED RELEASE

RouteORAL

Active ingredient(s)GUAIFENESIN, DEXTROMETHORPHAN HYDROBROMIDE

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

60000-057-65 — 1 BOTTLE in 1 CARTON (60000-057-65) / 14 TABLET, EXTENDED RELEASE in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

59779-275 — acetaminophen, guaifenesin, phenylephrine HCl, 59779-335 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 59779-384 — dextromethorphan polistirex, 59779-459 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 59779-603 — acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl, 59779-648 — Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 59779-656 — acetaminophen, dextromethorphan hbr, phenylephrine hcl, 59779-709 — dextromethorphan polistirex, 59779-763 — Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, Phenylephrine HCl, 59779-958 — dextromethorphan polistirex, 60000-058 — Guaifenesin and Dextromethorphan HBr, 60687-817 — Guaifenesin and Dextromethorphan, 60687-828 — Guaifenesin and Dextromethorphan, 60687-852 — Guaifenesin, 60687-863 — Guaifenesin, 60687-874 — Guaifenesin, 61504-204 — Guaifenesin, 61787-070 — benzocaine and dextromethorphan HBr, 61787-515 — Dextromethorphan Hydrobromide and Guaifenesin, 62011-0060 — 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.