Cold and Flu

NDC 63868-140 · QUALITY CHOICE (Chain Drug Marketing Association)

Generic nameAcetaminophen, Dextromethorphan Hydrobromide, 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

63868-140-08 — 237 mL in 1 BOTTLE, PLASTIC (63868-140-08)

63868-140-12 — 355 mL in 1 BOTTLE, PLASTIC (63868-140-12)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

63868-003 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 63868-020 — Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride, 63868-032 — Acetaminophen, Caffeine, Pyrilamine maleate, 63868-071 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 63868-081 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 63868-082 — Acetaminophen, 63868-084 — Acetaminophen, 63868-102 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 63868-103 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 63868-119 — Acetaminophen, Diphenhydramine HCl, 63868-174 — Acetaminophen, 63868-175 — Acetaminophen, 63868-186 — acetaminophen, 63868-210 — Acetaminophen, Diphenhydramine HCl, 63868-234 — Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate, 63868-235 — Dextromethorphan HBr, Guaifenesin, 63868-291 — ACETAMINOPHEN, DIPHENHYDRAMINE, PHENYLEPHRINE, 63868-292 — Dextromethorphan Hydrobromide, Doxylamine Succinate, 63868-325 — Acetaminophen and Diphenhydramine Hydrochloride, 63868-418 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, +4482 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