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Mucus Relief

NDC 53942-204 · Demoulas Super Markets, Inc

Generic nameGuaifenesin
Dosage formTABLET, EXTENDED RELEASE
RouteORAL
Active ingredient(s)GUAIFENESIN
Strength1200 mg/1
Pharmacologic classDecreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE]
Marketing categoryANDA

Packages

53942-204-02 — 1 BLISTER PACK in 1 CARTON (53942-204-02) / 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

53145-697 — DEXTROMETHORPHAN HBr, GUAIFENESIN, PHENYLEPHRINE HCL, 53163-104 — Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 53163-113 — Dextromethorphan HBr, Guaifenesin, 53209-1003 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride, 53209-1004 — Acetaminophen, Guaifenesin, and Phenylephrine Hydrochloride, 53345-021 — acetaminophen, dextromethorphan hydrobromide, Guaifenesin, phenylephrine hydrochloride, 53345-034 — Maximum Strength-Cough and Chest Congestion DM, 53499-0232 — GUAIFENESIN, 53499-5295 — GUAIFENESIN, 53942-203 — Guaifenesin, 53942-503 — DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, 53942-504 — DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE, 53942-515 — ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE, 53942-516 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE, 53942-517 — DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE, 53942-518 — DEXTROMETHORPHAN HBR, GUAIFENESIN, 53943-163 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 53943-167 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 53943-175 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 53943-178 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, +1437 more

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