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Foster and Thrive childrens cold cough relief dm

NDC 70677-1287 · Strategic Sourcing Services 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

70677-1287-1 — 1 BOTTLE in 1 CARTON (70677-1287-1) / 118 mL in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70677-1032 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 70677-1033 — Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine succinate, 70677-1035 — dextromethorphan hydrobromide, guaifenesin, 70677-1036 — Dextromethorphan HBr, Guaifenesin, 70677-1049 — Guaifenesin, Dextromethorphan HBr, 70677-1050 — Guaifenesin, Dextromethorphan HBr, 70677-1055 — Dextromethorphan Hydrobromide / Guaifenesin, 70677-1185 — Dextromethorphan HBr, Guaifenesin, 70677-1187 — Dextromethorphan HBr Guaifenesin Phenylephrine HCl, 70677-1261 — Dextromethorphan HBr Guaifenesin, 70677-1313 — acetaminophen, dextromethorphan hydrobromide, 70692-181 — Dextromethorphan Hydrobromide, Guaifenesin, 70692-778 — Dextromethorphan hydrobromide, 70692-836 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride, 70692-837 — Acetaminophen, Dextromethorphan hydrobromide, Doxylamine succinate, Phenylephrine hydrochloride, 70893-0011 — DEXTROMETHORPHAN HYDROBROMIDE, 70893-0012 — DEXTROMETHORPHAN HYDROBROMIDE, 71141-179 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 71141-180 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 71179-003 — Acetaminophen, Dextromethorphan hydrobromide and Doxylamine Succinate, +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