Mucolyte

NDC 57237-360 · Rising Pharma Holdings, Inc.

Generic nameGuaifenesin, Dextromethorphan HBr

Dosage formLIQUID

RouteORAL

Active ingredient(s)GUAIFENESIN, DEXTROMETHORPHAN HYDROBROMIDE

Strength10; 100 mg/5mL; mg/5mL

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

57237-360-12 — 118 mL in 1 BOTTLE (57237-360-12)

57237-360-16 — 473 mL in 1 BOTTLE (57237-360-16)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

56062-459 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 56062-502 — brompheniramine maleate, dextromethorphan hydrobromide, 56062-607 — dextromethorphan hydrobromide, guaifenesin, 56062-614 — guaifenesin, pseudoephedrine hydrochloride, 56062-656 — acetaminophen, dextromethorphan HBr, Phenylephrine HCl, 56062-763 — Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate, Phenylephrine Hydrochloride, 56062-987 — Brompheniramine maleate, Dextromethorphan HBr, Phenylephrine HCl, 57237-312 — Dextromethorphan HBr. and Guaifenesin, 57237-313 — Dextromethorphan HBr. and Guaifenesin, 57237-359 — Guaifenesin, 57243-501 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, 57243-502 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, 57243-503 — DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, 57243-506 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE, 57243-603 — Acetaminophen, Dextromethorphan HBr and Doxylamine Succinate, 57243-604 — ACETAMINOPHEN, DEXTROMETHORPHAN HBr, PHENYLEPHRINE HCl, 57344-163 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 57344-203 — Guaifenesin, 57483-270 — Guaifenesin Extended-Release, 57483-280 — Guaifensin Extended-Release, +2508 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.