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topcare nite time cold and flu

NDC 36800-291 · Topco Associates LLC

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

36800-291-40 — 355 mL in 1 BOTTLE (36800-291-40)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

36000-360 — phenylephrine hydrochloride, 36000-362 — phenylephrine hydrochloride, 36000-372 — Acetaminophen, 36800-037 — Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 36800-095 — Acetaminophen and Diphenhydramine Hydrochloride, 36800-143 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 36800-161 — Acetaminophen, 36800-202 — Acetaminophen, 36800-219 — dextromethorphan hydrobromide, guaifenesin, 36800-279 — cocoa butter, phenylephrine HCl, 36800-297 — Acetaminophen, Chlorpheniramine maleate, Dextromethorphan hydrobromide, 36800-298 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 36800-307 — acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, phenylephrine hydrochloride, 36800-320 — ACETAMINOPHEN and PHENYLEPHRINE HYDROCHLORIDE, 36800-322 — ACETAMINOPHEN and PHENYLEPHRINE HYDROCHLORIDE, 36800-335 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 36800-369 — Acetaminophen, 36800-391 — Acetaminophen, Caffeine, Pyrilamine maleate, 36800-441 — Doxylamine succinate, 36800-449 — 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