Skip to main content

Mucus Relief Cold and Flu All In One

NDC 36800-298 · TOPCARE

Generic nameACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE
Dosage formTABLET, COATED
RouteORAL
Active ingredient(s)ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE
Strength325; 10; 200; 5 mg/1; mg/1; mg/1; mg/1
Pharmacologic classAdrenergic alpha1-Agonists [MoA], Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA], alpha-1 Adrenergic Agonist [EPC]
Marketing categoryOTC MONOGRAPH DRUG

Packages

36800-298-04 — 2 BLISTER PACK in 1 CARTON (36800-298-04) / 10 TABLET, COATED in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

36800-037 — Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 36800-095 — Acetaminophen and Diphenhydramine Hydrochloride, 36800-143 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 36800-161 — Acetaminophen, 36800-202 — Acetaminophen, 36800-219 — dextromethorphan hydrobromide, guaifenesin, 36800-226 — Guaifenesin, 36800-279 — cocoa butter, phenylephrine HCl, 36800-291 — Acetaminophen, dextromethorphan HBr, doxylamine succinate, phenylephrine HCl, 36800-297 — Acetaminophen, Chlorpheniramine maleate, Dextromethorphan hydrobromide, 36800-307 — acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, phenylephrine hydrochloride, 36800-320 — ACETAMINOPHEN and PHENYLEPHRINE HYDROCHLORIDE, 36800-322 — ACETAMINOPHEN and PHENYLEPHRINE HYDROCHLORIDE, 36800-335 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 36800-369 — Acetaminophen, 36800-391 — Acetaminophen, Caffeine, Pyrilamine maleate, 36800-449 — Acetaminophen, 36800-450 — Acetaminophen, 36800-455 — Acetaminophen, 36800-459 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, +5267 more

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