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Guaifenesin

NDC 60687-874 · American Health Packaging

Generic nameGuaifenesin
Dosage formSOLUTION
RouteORAL
Active ingredient(s)GUAIFENESIN
Strength300 mg/15mL
Pharmacologic classDecreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE]
Marketing categoryOTC MONOGRAPH DRUG

Packages

60687-874-16 — 10 TRAY in 1 CASE (60687-874-16) / 10 CUP, UNIT-DOSE in 1 TRAY (60687-874-50) / 15 mL in 1 CUP, UNIT-DOSE (60687-874-44)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

59726-734 — Guaifenesin, 59779-275 — acetaminophen, guaifenesin, phenylephrine HCl, 59779-603 — acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl, 59779-648 — Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 60000-057 — Guaifenesin and Dextromethorphan HBr, 60000-058 — Guaifenesin and Dextromethorphan HBr, 60687-817 — Guaifenesin and Dextromethorphan, 60687-828 — Guaifenesin and Dextromethorphan, 60687-852 — Guaifenesin, 60687-863 — Guaifenesin, 61504-204 — Guaifenesin, 61787-515 — Dextromethorphan Hydrobromide and Guaifenesin, 62011-0060 — Guaifenesin, 62011-0475 — Guaifenesin and Pseudoephedrine Hydrochloride, 62207-569 — GUAIFENESIN, 62207-570 — GUAIFENESIN, 62207-827 — Guaifenesin and Pseudoephedrine HCl, 62207-828 — Guaifenesin and Pseudoephedrine HCl, 62207-839 — GUAIFENESIN, 62207-840 — GUAIFENESIN, +1437 more

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