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DAYTIME COLD AND FLU

NDC 41226-693 · Kroger Company

Generic nameDEXTROMETHORPHAN HYDROBROMIDE, ACETAMINOPHEN, PHENYLEPHRINE HYDROCHLORIDE
Dosage formCAPSULE, LIQUID FILLED
RouteORAL
Active ingredient(s)DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE, ACETAMINOPHEN
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

41226-693-24 — 2 BLISTER PACK in 1 CARTON (41226-693-24) / 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

41226-340 — Acetaminophen, 41226-341 — ACETAMINOPHEN, 41226-370 — ACETAMINOPHEN, ASPIRIN AND CAFFEINE, 41226-541 — ACETAMINOPHEN, DIPHENHYDRAMINE, PHENYLEPHRINE, 41226-625 — ACETAMINOPHEN, PHENYLEPHRINE HCL, DEXTROMETHORPHAN HBR, GUAIFENESIN, 41226-626 — ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HCL, 41226-628 — ACETAMINOPHEN, DEXTROMETHORPHAN HBr, GUAILFENESIN,PHENLYEPHRINE HCL, 41226-673 — Acetaminophen, 41226-674 — Acetaminophen, Dextromethorphan HBr, 41226-675 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 41226-694 — DEXTROMETHORPHAN HYDROBROMIDE, ACETAMINOPHEN, DOXYLAMINE SUCCINATE, 41226-697 — ACETAMINOPHEN, 41226-699 — Acetaminophen, 41226-704 — Acetaminophen, 41226-716 — Acetaminophen, Ibuprofen, 41226-739 — Dextromethorphan HBr and Guaifenesin, 41226-750 — Acetaminophen, Dextromethrophan HBr, Doxylamine succinate, 41226-766 — Acetaminophen, Dextromethrophan HBr, Guaifenesin, Phenylephrine HCl, 41226-767 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, Phenylephrine HCl, 41226-772 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, +4867 more

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