Nitetime Cold and Flu

NDC 41250-763 · Meijer Distribution Inc

Generic nameAcetaminophen, Dextromethorphan HBr, Doxylamine Succinate, Phenylephrine HCl

Dosage formSOLUTION

RouteORAL

Active ingredient(s)ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HYDROCHLORIDE

Strength650; 20; 12.5; 10 mg/30mL; mg/30mL; mg/30mL; mg/30mL

Pharmacologic classAdrenergic alpha1-Agonists [MoA], Antihistamine [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], alpha-1 Adrenergic Agonist [EPC]

Marketing categoryOTC MONOGRAPH DRUG

Packages

41250-763-40 — 355 mL in 1 BOTTLE (41250-763-40)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

41250-631 — Acetaminophen, 41250-638 — Acetaminophen, Chlorpheniramine maleate, Dextromethorphan HBr, 41250-643 — acetaminophen, dextromethorphan HBr, guaifenesin, phenylephrine HCl, 41250-650 — Acetaminophen, 41250-656 — acetaminophen, dextromethorphan Hbr, Phenylephrine HCl, 41250-658 — Acetaminophen, 41250-663 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 41250-692 — Acetaminophen, Chlorpheniramine maleate, 41250-748 — Dextromethorphan HBr and Guaifenesin, 41250-758 — dextromethorphan hydrobromide, doxylamine succinate, 41250-766 — Acetaminophen, 41250-776 — dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride, 41250-802 — Acetaminophen, 41250-811 — Acetaminophen, dextromethorphan HBr, doxylamine succinate, phenylephrine HCl, 41250-812 — dextromethorphan HBr, guaifenesin, 41250-869 — Acetaminophen, Dextromethorphan HBr, Triprolidine HCl, 41250-877 — Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, Phenylephrine HCl, 41250-899 — Dextromethorphan polistirex, 41250-944 — glycerin, phenylephrine HCl, pramoxine HCl, white petrolatum, 41250-946 — Acetaminophen, +4930 more

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

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels