Skip to main content

Vicks ZzzQuil

NDC 69423-985 · The Procter & Gamble Manufacturing Company

Generic nameDiphenhydramine Hydrochloride and Acetaminophen
Dosage formLIQUID
RouteORAL
Active ingredient(s)DIPHENHYDRAMINE HYDROCHLORIDE, ACETAMINOPHEN
Strength1000; 50 mg/30mL; mg/30mL
Pharmacologic classHistamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
Marketing categoryOTC MONOGRAPH DRUG

Packages

69423-985-02 — 2 BOTTLE in 1 CARTON (69423-985-02) / 354 mL in 1 BOTTLE

69423-985-12 — 354 mL in 1 BOTTLE (69423-985-12)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

69423-830 — Diphenhydramine HCl, 69423-833 — Acetaminophen, 69423-834 — Acetaminophen, Diphenhydramine HCl, 69423-843 — Acetaminophen, Dextromethorphan HBr, 69423-844 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 69423-899 — Acetaminophen, Chlorpheniramine maleate, and Dextromethorphan Hydrobromide, 69423-964 — acetaminophen, phenylephrine hydrochloride, dextromethorphan hydrobromide, and guaifenesin, 69423-968 — Acetaminophen, Dextromethrophan, Doxylamine succinate, Phenylephrine HCl, 69423-972 — Acetaminophen, Dextromethorphan, 69423-973 — Acetaminophen, Dextromethorphan Hydrobromide, and Doxylamine succinate, 69423-986 — Acetaminophen, Phenylephrine Hydrochloride, Doxylamine Succinate, and Dextromethorphan Hydrobromide, 69423-987 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride, 69423-989 — acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, and phenylephrine hydrochloride, 69423-990 — acetaminophen, phenylephrine hydrochloride, dextromethorphan hydrobromide, and guaifenesin, 69423-994 — Acetaminophen, Dextromethorphan Hydrobromide, and Phenylephrine Hydrochloride, 69423-995 — Acetaminophen, Dextromethorphan Hydrobromide, and Doxylamine Succinate, 69452-205 — IBUPROFEN, DIPHENHYDRAMINE HCL, 69452-264 — IBUPROFEN, DIPHENHYDRAMINE HCL, 69452-322 — Diphenhydramine HCl, 69452-376 — Itch Relief Gel, +4329 more

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