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Cold and Flu Relief

NDC 55910-599 · Dolgencorp, Inc. (DOLLAR GENERAL & REXALL)

Generic nameAcetaminophen, Dextromethorphan HBr, Doxylamine Succinate
Dosage formCAPSULE, LIQUID FILLED
RouteORAL
Active ingredient(s)ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE
Strength325; 15; 6.25 mg/1; mg/1; mg/1
Pharmacologic classAntihistamine [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]
Marketing categoryOTC MONOGRAPH DRUG

Packages

55910-599-48 — 48 BLISTER PACK in 1 CARTON (55910-599-48) / 1 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

55910-505 — Dextromethorphan HBr, Guaifenesin, 55910-506 — Acetaminophen, 55910-508 — acetaminophen, ibuprofen, 55910-509 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 55910-515 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride, 55910-529 — Acetaminophen, Guaifenesin, Phenylephrine HCl, 55910-533 — Dextromethorphan HBr, Guaifenesin, 55910-537 — dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, 55910-575 — dextromethorphan HBr, guaifenesin, 55910-576 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, 55910-608 — acetaminophen, dextromethorphan hydrobromide, 55910-613 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 55910-639 — acetaminophen, aspirin, caffeine, 55910-655 — Acetaminophen and Diphenhydramine HCl, 55910-656 — acetaminophen, dextromethorphan Hbr, Phenylephrine HCl, 55910-661 — Acetaminophen, 55910-686 — Acetaminophen, Aspirin, Caffeine, 55910-689 — Chlorpheniramine Maleate, Dextromethorphan HBr, 55910-697 — Acetaminophen, 55910-701 — Acetaminophen, +4482 more

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