topcare childrens cold cough

NDC 76162-099 · Topco Associates LLC

Generic namebrompheniramine maleate, dextromethorphan hydrobromide

Dosage formSOLUTION

RouteORAL

Active ingredient(s)BROMPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE

Strength2; 10 mg/10mL; mg/10mL

Pharmacologic classSigma-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

76162-099-26 — 1 BOTTLE in 1 CARTON (76162-099-26) / 118 mL in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

76095-012 — Guaifensin, Dextromethorphan, 76117-001 — CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE, 76162-000 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride, 76162-008 — Mucus Relief DM, 76162-026 — Nite Time Cold and Flu Relief, 76162-032 — GUAIFENESIN AND DEXTROMETHORPHAN HBR, 76162-040 — Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 76162-050 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 76162-057 — Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 76162-065 — Daytime Cold and Flu Relief, 76162-198 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, 76162-202 — acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, phenylephrine hydrochloride, 76162-294 — Dextromethorphan HBr, Guaifensin, 76162-483 — acetaminophen, dextromethorphan hydrobromide, 76162-500 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, 76162-598 — acetaminophen, dextromethorphan hydrobromide, 76162-599 — acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, 76162-600 — dextromethorphan hydrobromide, guaifenesin, 76162-619 — acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, 76162-628 — Dextromethorphan HBr, Guaifenesin, +1981 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