NIGHTTIME COLD AND FLU RELIEF

NDC 68016-878 · Chain Drug Consortium, LLC

Generic nameAcetaminophen, Dextromethorphan HBr and Doxylamine Succinate

Dosage formCAPSULE

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

68016-878-16 — 8 BLISTER PACK in 1 CARTON (68016-878-16) / 2 CAPSULE in 1 BLISTER PACK

68016-878-24 — 12 BLISTER PACK in 1 CARTON (68016-878-24) / 2 CAPSULE in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68016-303 — Acetaminophen, 68016-543 — Acetaminophen, 68016-654 — Acetaminophen Diphenhydramine HCl, 68016-674 — Guaifenesin, Dextromethorphan HBr, 68016-734 — Acetaminophen, 68016-740 — Dextromethorphan HBr, Guaifenesin, 68016-742 — Dextromethorphan HBr, 68016-744 — Dextromethorphan HBr, Guaifenesin, 68016-797 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 68016-877 — Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride, 68047-129 — Brompheniramine Maleate, Dextromethorphan Hydrobromide and Phenylephrine Hydrochloride, 68047-143 — Brompheniramine Maleate, Dextromethorphan Hydrobromide and Phenylephrine Hydrochloride, 68047-186 — Chlorpheniramine Maleate, Dextromethorphan Hydrobromide and Phenylephrine Hydrochloride, 68047-721 — butalbital and acetaminophen, 68047-752 — butalbital and acetaminophen, 68047-753 — butalbital and acetaminophen, 68071-2494 — Hydrocodone Bitartrate and Acetaminophen, 68071-2645 — Hydrocodone Bitartrate and Acetaminophen, 68071-3249 — Butalbital, Acetaminophen, and Caffeine, 68071-3437 — 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.