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MUCUS RELIEF

NDC 71335-2032 · Bryant Ranch Prepack

Generic nameGuaifenesin
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

71335-2032-1 — 30 TABLET in 1 BOTTLE (71335-2032-1)

71335-2032-2 — 20 TABLET in 1 BOTTLE (71335-2032-2)

71335-2032-3 — 50 TABLET in 1 BOTTLE (71335-2032-3)

71335-2032-4 — 60 TABLET in 1 BOTTLE (71335-2032-4)

71335-2032-5 — 40 TABLET in 1 BOTTLE (71335-2032-5)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70677-1273 — guaifenesin, pseudoephedrine hydrochloride, 70677-1291 — guaifenesin, 70692-181 — Dextromethorphan Hydrobromide, Guaifenesin, 70692-836 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride, 71179-002 — Guaifenesin, 71179-011 — Guaifenesin and Dextromethorphan HBr, 71205-624 — Codeine Phosphate and Guaifenesin, 71309-461 — GUAIFENESIN, 71335-1035 — Guaifenesin, 71335-1928 — Guaifenesin and Dextromethorphan HBr, 71335-2216 — Dextromethorphan Hydrobromide / Guaifenesin, 71335-2642 — Guaifenesin, 71335-9616 — Guaifenesin, 71399-0024 — Guaifenesin, 71399-0025 — Dextromethorphan HBr, Guaifenesin, 71399-0026 — Dextromethorphan HBr, Guaifenesin, 71399-0054 — Guaifenesin, 71610-098 — Guaifenesin 200 mg, 71610-434 — Guaifenesin, 71610-499 — 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.