Skip to main content

topcare nite time cold and flu relief

NDC 36800-335 · Topco Associates LLC

Generic nameAcetaminophen, Dextromethorphan HBr, Doxylamine succinate
Dosage formSOLUTION
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

36800-335-34 — 237 mL in 1 BOTTLE (36800-335-34)

36800-335-40 — 355 mL in 1 BOTTLE (36800-335-40)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

36800-143 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 36800-161 — Acetaminophen, 36800-202 — Acetaminophen, 36800-219 — dextromethorphan hydrobromide, guaifenesin, 36800-291 — Acetaminophen, dextromethorphan HBr, doxylamine succinate, 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, 36800-369 — Acetaminophen, 36800-391 — Acetaminophen, Caffeine, Pyrilamine maleate, 36800-441 — Doxylamine succinate, 36800-449 — Acetaminophen, 36800-450 — Acetaminophen, 36800-455 — Acetaminophen, 36800-459 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 36800-466 — Acetaminophen, Diphenhydramine HCl, 36800-474 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 36800-484 — 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.