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Daytime Cold and Flu

NDC 55319-960 · Family Dollar (FAMILY WELLNESS)

Generic nameAcetaminophen, Dextromethorphan HBr, Phenylephrine HCl
Dosage formLIQUID
RouteORAL
Active ingredient(s)ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE
Strength650; 20; 10 mg/30mL; mg/30mL; mg/30mL
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

55319-960-08 — 245 mL in 1 BOTTLE, PLASTIC (55319-960-08)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 55319-933 — ACETAMINOPHEN, DEXTROMETHORPHAN, PHENYLEPHRINE HCL, 55319-934 — ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HCL, 55319-954 — Acetaminophen Dextromethorphan HBr, 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, 55505-230 — Acetaminophen, Dextromethorphan Hydrobromide, and Guaifenesin, 55505-231 — Dextromethorphan Hydrobromide, and Guaifenesin, 55579-110 — ACETAMINOPHEN, +4867 more

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