MAXIMUM STRENGHT DAY COLD AND FLU FORMULA

NDC 55319-933 · FAMILY DOLLAR

Generic nameACETAMINOPHEN, DEXTROMETHORPHAN, PHENYLEPHRINE HCL

Dosage formCAPSULE, LIQUID FILLED

RouteORAL

Active ingredient(s)ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE

Strength325; 10; 5 mg/1; mg/1; mg/1

Pharmacologic classAdrenergic alpha1-Agonists [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

55319-933-22 — 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (55319-933-22)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

55319-734 — Guaifenesin, Dextromethorphan HBr, 55319-740 — Dextromethorphan HBr, Guaifenesin, 55319-741 — Guaifenesin, Dextromethorphan HBr, 55319-751 — Acetaminophen, 55319-754 — chlorpheniramine maleate, dextrometrorphan HBr, 55319-815 — Acetaminophen, Guaifenesin, Phenylephrine HCl, 55319-890 — Dextromethorphan Hydrobromide / Guaifenesin, 55319-924 — Dextromethorphan HBr, Guaifenesin, 55319-926 — Acetaminophen, Dextromethorphan Hydrobromide and Doxylamine succinate, 55319-930 — Acetaminophen, 55319-934 — ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HCL, 55319-954 — Acetaminophen Dextromethorphan HBr, 55319-960 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 55319-967 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 55319-968 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, 55319-970 — Acetaminophen, Aspirin, Caffeine, 55319-979 — Acetaminophen, Pamabrom, Pyrilamine Maleate, 55319-981 — Glycerin, Petrolatum, Phenylephrine HCL, Pramoxine HCL, 55505-217 — Acetaminophen, Dextromethorphan Hydrobromide, and Guaifenesin, 55505-220 — Dextromethorphan Hydrobromide, and Guaifenesin, +4867 more

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