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basic care daytime severe cold and flu

NDC 72288-357 · Amazon.com Services LLC

Generic nameacetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride
Dosage formTABLET, FILM 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

72288-357-62 — 12 BLISTER PACK in 1 CARTON (72288-357-62) / 2 TABLET, FILM COATED in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

72288-189 — acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, phenylephrine hydrochloride, 72288-219 — dextromethorphan hydrobromide, guaifenesin, 72288-220 — Guaifenesin and Dextromethorphan HBr, 72288-252 — acetaminophen, aspirin, caffeine, 72288-293 — Dextromethorphan HBr, Guaifenesin, 72288-295 — acetaminophen, aspirin, caffeine, 72288-298 — Guaifenesin, 72288-300 — Acetaminophen, 72288-303 — Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride, 72288-335 — Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine succinate, 72288-374 — Acetaminophen, Aspirin, Caffeine, 72288-376 — acetaminophen, aspirin and caffeine, 72288-384 — dextromethorphan polistirex, 72288-403 — Acetaminophen, 72288-405 — Acetaminophen, 72288-437 — Acetaminophen, Diphenhydramine HCl, 72288-449 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, 72288-459 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 72288-463 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride, 72288-494 — dextromethorphan polistirex, +5267 more

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