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mucus relief

NDC 11822-2123 · Rite Aid 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

11822-2123-0 — 1 BLISTER PACK in 1 CARTON (11822-2123-0) / 20 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BLISTER PACK

11822-2123-1 — 2 BLISTER PACK in 1 CARTON (11822-2123-1) / 20 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

11673-972 — ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL, 11673-978 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 11822-0046 — Guaifenesin and Pseudoephedrine HCL, 11822-0527 — Acetaminophen, Guaifenesin and Phenylephrine HCl, 11822-0640 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 11822-0710 — acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl, 11822-0733 — Guaifenesin, Dextromethorphan HBr, 11822-1332 — Dextromethorphan Hydrobromide, Guaifenesin, 11822-1630 — dextromethorphan hydrobromide, guaifenesin, 11822-1812 — dextromethorphan HBr, guaifenesin, 11822-2219 — dextromethorphan hydrobromide, guaifenesin, 11822-3120 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, 11822-3252 — Guaifenesin, 11822-4260 — Guaifenesin, 11822-5031 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 11822-5050 — Dextromethorphan Hydrobromide Guaifenesin, 11822-5160 — Acetaminophen, Guaifenesin, Phenylephrine HCl, 11822-5462 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 11822-6179 — ACETAMINOPHEN, DEXTROMETHORPHAN HBr, GUAIFENESIN, PHENYLEPHRINE HCl, 11822-7340 — Guaifenesin, Dextromethorphan HBr, +1437 more

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