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Vicks NyQuil

NDC 84126-381 · The Procter & Gamble Manufacturing Company

Generic nameDoxylamine succinate
Dosage formCAPSULE, LIQUID FILLED
RouteORAL
Active ingredient(s)DOXYLAMINE SUCCINATE
Strength6.25 mg/1
Pharmacologic classAntihistamine [EPC], Histamine Receptor Antagonists [MoA]
Marketing categoryOTC MONOGRAPH DRUG

Packages

84126-381-24 — 2 BLISTER PACK in 1 CARTON (84126-381-24) / 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

84126-308 — Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine succinate, 84126-314 — Acetaminophen, Dextromethorphan Hydrobromide, and Doxylamine succinate, 84126-342 — Acetaminophen, Dextromethorphan Hydrobromide, and Doxylamine succinate, 84126-345 — Doxylamine Succinate, 84126-346 — Doxylamine Succinate, 84126-353 — Acetaminophen, Doxylamine Succinate, Dextromethorphan Hydrobromide, 84126-357 — Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine succinate, 84126-360 — Acetaminophen, Doxylamine Succinate, Dextromethorphan HBr, 84126-364 — Acetaminophen, Pseudoephedrine HCl, Doxylamine Succinate, Dextromethorphan HBr, 84126-374 — Acetaminophen, Doxylamine succinate, 84324-019 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, Doxylamine succinate, 84324-024 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, Doxylamine succinate, 84379-276 — Acetaminophen, Dextromethorphan HBr and Doxylamine succinate, 84379-444 — acetaminophen, dextromethorphan HBr, Doxylamine Succinate, 85766-177 — Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine succinate, 85786-602 — Acetaminophen 325 mg, Dextromethorphan HBr 15 mg, Doxylamine Succinate 6.25 mg, 85828-418 — Nighttime Cold and Flu Relief, 85828-439 — Doxylamine Succinate, 85828-750 — Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine succinate, 85828-775 — Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, Phenylephrine HCl, +423 more

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