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Walgreen High Blood Pressure Nighttime

NDC 0363-6210 · WALGREENS CO.

Generic nameAcetaminophen, Dextromethorphan Hydrobromide, and Doxylamine succinate
Dosage formLIQUID
RouteORAL
Active ingredient(s)ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE
Strength650; 30; 12.5 mg/30mL; mg/30mL; mg/30mL
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

0363-6210-08 — 236 mL in 1 BOTTLE, PLASTIC (0363-6210-08)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0363-6002 — acetaminophen, 0363-6005 — Dextromethorphan Hydrobromide and Guaifenesin, 0363-6020 — acetaminophen, 0363-6028 — Acetaminophen, Guaifenesin, Phenylephrine HCl, 0363-6048 — Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 0363-6142 — acetaminophen, dextromethorphan HBr, doxylamine succinate, and phenylephrine hydrochloride, 0363-6150 — Acetaminophen, Guaifenesin, Phenylephrine HCl, 0363-6171 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 0363-6190 — Acetaminophen, Dextromethorphan, 0363-6199 — acetaminophen, ibuprofen, 0363-6238 — GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE AND DEXTROMETHORPHAN HYDROBROMIDE, 0363-6248 — Doxylamine Succinate, Phenylephrine Hydrochloride and Dextromethorphan Hydrobromide, 0363-6251 — Doxylamine Succinate, 0363-6300 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, 0363-6504 — Acetaminophen and Dextromethorphan Hydrobromide, 0363-6555 — Acetaminophen, 0363-6681 — Guaifenesin and Dextromethorphan Hydrobromide, 0363-6684 — Acetaminophen capsules 500mg (Minis-red opaque), 0363-6693 — Acetaminophen 250mg, Aspirin 250mg and Caffeine 65mg, 0363-6779 — 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.