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up and up mucus relief

NDC 11673-421 · Target Corporation

Generic nameguaifenesin
Dosage formTABLET, MULTILAYER, 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

11673-421-01 — 1 BLISTER PACK in 1 CARTON (11673-421-01) / 20 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

10202-740 — Dextromethorphan HBr, Guaifenesin, 10956-059 — Guaifenesin, 10956-845 — Guaifenesin, 10956-846 — Dextromethorphan Hydrobromide / Guaifenesin, 11383-311 — Dextromethorphan HBr, Guaifenesin, 11523-0094 — Acetaminophen, Guaifenesin, 11673-267 — Guaifenesin and Dextromethorphan HBr, 11673-337 — Dextromethorphan HBr, Guaifenesin, Phenylephrine HCI, 11673-347 — acetaminophen, dextromethorphan HBr, guaifenesin, phenylephrine HCl, 11673-410 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 11673-539 — Guaifenesin, 11673-627 — Dextromethorphan HBr, Guaifenesin, 11673-716 — dextromethorphan hydrobromide, guaifenesin, 11673-731 — Guaifenesin, 11673-732 — Guaifenesin, 11673-738 — dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride, 11673-773 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 11673-775 — Dextromethorphan HBr, Guaifenesin, 11673-840 — Guaifenesin, 11673-961 — acetaminophen, 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.