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basic care nighttime severe cold and flu

NDC 72288-721 · Amazon.com Services LLC

Generic nameacetaminophen, dextromethorphan hydrobromide, doxylamine succinate, phenylephrine hydrochloride
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HYDROCHLORIDE
Strength325; 10; 6.25; 5 mg/1; mg/1; mg/1; mg/1
Pharmacologic classAdrenergic alpha1-Agonists [MoA], Antihistamine [EPC], Histamine Receptor Antagonists [MoA], 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

72288-721-62 — 12 BLISTER PACK in 1 CARTON (72288-721-62) / 2 TABLET, FILM COATED in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

72288-603 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, 72288-631 — dextromethorphan hydrobromide, guaifenesin, 72288-634 — Acetaminophen, 72288-639 — Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate, Phenylephrine Hydrochloride, 72288-648 — Phenylephrine hydrochloride, 72288-649 — Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride, 72288-656 — acetaminophen, dextromethorphan Hbr, Phenylephrine HCl, 72288-670 — Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine succinate, 72288-692 — Acetaminophen, 72288-698 — Acetaminophen, 72288-766 — Acetaminophen, 72288-800 — cocoa butter, phenylephrine HCl, 72288-812 — dextromethorphan HBr, guaifenesin, 72288-866 — acetaminophen, dextromethorphan Hbr, Phenylephrine HCl, 72288-899 — Dextromethorphan polistirex, 72288-946 — Acetaminophen, 72288-958 — dextromethorphan polistirex, 72288-959 — Acetaminophen, 72288-964 — Acetaminophen, Diphenhydramine hydrochloride, Phenylephrine hydrochloride, 72288-975 — Acetaminophen, +4930 more

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