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Mucus Relief 600 mg

NDC 53041-190 · Guardian Drug Company

Generic nameGuaifenesin
Dosage formTABLET, EXTENDED RELEASE
RouteORAL
Active ingredient(s)GUAIFENESIN
Strength600 mg/1
Pharmacologic classDecreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE]
Marketing categoryANDA

Packages

53041-190-16 — 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (53041-190-16)

53041-190-20 — 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (53041-190-20)

53041-190-32 — 2 BLISTER PACK in 1 CARTON (53041-190-32) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

53041-190-38 — 4 BLISTER PACK in 1 CARTON (53041-190-38) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

52083-624 — Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride, 52083-630 — Dextromethorphan HBr, Guaifenesin, 52083-632 — guaifenesin, phenylephrine hydrochloride, dextromethorphan hydrobromide, 52083-639 — dextromethorphan, guaifenesin, and phenylephrine, 52083-641 — Dextromethorphan Hbr, Guiafenesin, Phenylephrine HCl, 52083-646 — Dextromethorphan HBr ,Guaifenesin ,Phenylephrine HCl, 52083-653 — GUAIFENESIN, PHENYLEPHRINE HCL,DEXTROMETHORPHAN HYDROBROMIDE, 52083-655 — Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride, 52083-660 — dextromethorphan hydrobromide, glycerol guaiacolate, 52412-992 — DEXTROMETHORPHAN HYDROBROMIDE and GUAIFENESIN, 53041-191 — Guaifenesin, 53041-233 — Guaifenesin, 53041-234 — Guaifenesin, 53041-615 — Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 53041-616 — Acteaminophen, Guaifenesin, Phenylephrine HCl, 53041-617 — Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 53041-618 — Acteaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 53041-622 — Acteaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 53041-628 — Dextromethorphan HBr, Guaifenesin, 53113-514 — Dextromethorphan Hydrobromide, 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.