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Ultra Concentrated Nighttime COLD AND FLU

NDC 51013-668 · PuraCap Pharmaceutical LLC

Generic nameacetaminophen, dextromethorphan hydrobromide, doxylamine succinate
Dosage formCAPSULE, LIQUID FILLED
RouteORAL
Active ingredient(s)ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE
Strength325; 10; 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

51013-668-01 — 1 BLISTER PACK in 1 CARTON (51013-668-01) / 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50991-444 — Dextromethorphan HBr, Pheniramine Maleate, Phenylephrine HCl, 50991-535 — ACETAMINOPHEN, DEXTROMETHORPHAN HBr, GUAIFENESIN, PSEUDOEPHEDRINE HCl, 50991-626 — Doxylamine Succinate and Phenylephrine Hydrochloride, 50991-740 — Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride, 51013-169 — Acetaminophen, Dextromethorphan hydrobromide , Doxylamine succinate, Phenylephrine hydrochloride, 51013-174 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, 51013-175 — Acetaminophen, Phenylephrine hydrochloride, Doxylamine succinate, Dextromethorphan hydrobromide, 51013-320 — Acetaminophen, 51013-666 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, 51013-667 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, 51316-009 — Guaifenesin and Dextromethorphan HBR, 51316-060 — Guaifenesin and Dextromethorphan HBr, 51316-062 — Dextromethorphan Hydrobromide, Doxylamine succinate, 51316-065 — Guaifenesin and Dextromethorphan HBr, 51316-080 — Dextromethorphan HBr, 51316-081 — Dextromethorphan HBr, 51316-082 — dextromethorphan hydrobromide, guaifenesin, 51316-089 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, 51316-097 — Acetaminophen, 51316-098 — 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.