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Mucus Relief

NDC 54738-980 · Richmond Pharmaceuticals, Inc.

Generic nameGuaifenesin 200 mg
Dosage formTABLET
RouteORAL
Active ingredient(s)GUAIFENESIN
Strength200 mg/1
Marketing categoryOTC MONOGRAPH FINAL

Packages

54738-980-01 — 100 TABLET in 1 BOTTLE (54738-980-01)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

53943-319 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 53943-503 — DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, 53943-504 — DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE, 53943-507 — GUAIFENESIN, 53943-511 — GUAIFENESIN, 53943-512 — DEXTROMETHORPHANN Hbr, GUAIFENESIN, 53943-517 — DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE, 53943-518 — DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, 54257-277 — DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, 54257-776 — GUAIFENESIN, 54738-981 — Guaifenesin 400 mg, 54738-985 — Guaifenesin and Dextromethorphan HBr, 54859-011 — Dextromethorphan HBr, Guaifenesin, 54859-502 — Dextromethorphan, Guiafenesin, Pseudoephedrine HCl, 54859-505 — Dextromethorphan, Guaifenesin, 54859-506 — Dextromethorphan HBr, Guaifenesin, 54859-507 — Guaifenesin, 54859-509 — Dextromethorphan HBr, Guaifenesin, 54859-510 — Guaifenesin, 54859-517 — Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, +1437 more

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