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Vicks NyQuil ALLERGY

NDC 84126-346 · The Procter & Gamble Manufacturing Company

Generic nameDoxylamine Succinate
Dosage formLIQUID
RouteORAL
Active ingredient(s)DOXYLAMINE SUCCINATE
Strength6.25 mg/15mL
Pharmacologic classAntihistamine [EPC], Histamine Receptor Antagonists [MoA]
Marketing categoryOTC MONOGRAPH DRUG

Packages

84126-346-12 — 354 mL in 1 BOTTLE, PLASTIC (84126-346-12)

84126-346-24 — 2 BOTTLE, PLASTIC in 1 CARTON (84126-346-24) / 354 mL in 1 BOTTLE, PLASTIC

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

83324-158 — Acetaminophen Dextromethorphan HBr Doxylamine Succinate, 83324-159 — Acetaminophen Dextromethorphan HBr Doxylamine Succinate, 83324-163 — Acetaminophen Dextromethorphan HBr Doxylamine Succinate, 83324-164 — Acetaminophen Dextromethorphan HBr Doxylamine Succinate, 83324-224 — Acetaminophen, Dextromethorphan hydrobromide, Doxylamine succinate, Phenylephrine hydrochloride, 84126-305 — Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine succinate, 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, 84126-353 — 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, 84126-381 — 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, +423 more

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