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MUCUS RELIEF

NDC 72090-009 · Pioneer Life Sciences, LLC

FDA carries 2 listing records for this NDC; the most recent is shown.

Generic nameguaifenesin 400 mg
Dosage formTABLET
RouteORAL
Active ingredient(s)GUAIFENESIN
Strength400 mg/1
Pharmacologic classDecreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE]
Marketing categoryOTC MONOGRAPH DRUG

Packages

72090-009-01 — 200 TABLET in 1 BOTTLE (72090-009-01)

72090-009-02 — 300 TABLET in 1 BOTTLE (72090-009-02)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

72036-155 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 72036-167 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 72036-175 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 72036-199 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 72036-203 — Guaifenesin, 72036-204 — Guaifenesin, 72036-274 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 72036-297 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 72036-298 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 72036-980 — Guaifenesin and Dextromethorphan HBr, 72090-011 — Guaifenesin, 72090-012 — Guaifenesin, 72090-013 — guaifenesin 400 mg, 72090-019 — guaifenesin 400 mg, 72090-027 — Dextromethorphan HBr 20mg Guaifenesin 400mg, 72090-035 — guaifenesin 400 mg, 72090-044 — Guaifenesin 400 mg, 72162-1669 — Codeine Phosphate and Guaifenesin, 72162-2277 — Guaifenesin and Dextromethorphan Hydrobromide, 72162-2278 — 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.