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Mucus Relief

NDC 55910-732 · Dolgencorp, Inc. (DOLLAR GENERAL & REXALL)

FDA lists marketing as ended on 2026-08-28.
Generic nameGuaifenesin
Dosage formTABLET
RouteORAL
Active ingredient(s)GUAIFENESIN
Strength1200 mg/1
Pharmacologic classDecreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE]
Marketing categoryANDA

Packages

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

55910-432 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, 55910-505 — Dextromethorphan HBr, Guaifenesin, 55910-515 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride, 55910-529 — Acetaminophen, Guaifenesin, Phenylephrine HCl, 55910-533 — Dextromethorphan HBr, Guaifenesin, 55910-537 — dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, 55910-575 — dextromethorphan HBr, guaifenesin, 55910-576 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, 55910-613 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 55910-626 — Guaifenesin, 55910-733 — Guaifenesin, Dextromethorphan HBr, 55910-737 — acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl, 55910-739 — Guaifenesin, 55910-746 — dextromethorphan hydrobromide, guaifenesin, 55910-755 — Dextromethorphan HBr, Guaifenesin, 55910-757 — Acetaminophen, Guaifenesin, Phenylephrine HCL, 55910-774 — dextromethorphan hydrobromide, guaifenesin, 55910-776 — dextromethorphan hydrobromide, guaifenesin, 55910-886 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 55910-887 — 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.