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good sense childrens cold cough

NDC 68788-4094 · Preferred Pharmaceuticals Inc.

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

68788-4094-1 — 1 BOTTLE in 1 CARTON (68788-4094-1) / 118 mL in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68163-771 — Dextromethorphan HBr, 68163-774 — Dextromethorphan HBr, 68196-812 — dextromethorphan HBr, guaifenesin, 68196-999 — Guaifenesin and Dextromethorphan HBR, 68210-4210 — Acetaminophen, Dextromethorphan hydrobromide, Doxylamine succinate, Phenylephrine hydrochloride, 68210-5053 — Acetaminophen, Dextromethorphan Hydrobromide and Phenylephrine Hydrochloride, 68391-299 — Dextromethorphan HBr, Guaifenesin, 68391-711 — Dextromethorphan HBr, Guaifenesin, 68391-812 — dextromethorphan HBr, guaifenesin, 68436-120 — Sorbutuss, 68788-8100 — Promethazine Hydrochloride and Dextromethorphan Hydrobromide Oral Solution, 68788-8134 — Brompheniramine maleate, Dextromethorphan HBr, Phenylephrine HCl, 68788-8268 — dextromethorphan hydrobromide, guaifenesin, 68788-8300 — dextromethorphan hydrobromide, guaifenesin, 68788-8303 — dextromethorphan hydrobromide, guaifenesin, 68788-8331 — Brompheniramine maleate, Dextromethorphan HBr, Phenylephrine HCl, 68998-114 — Dextromethorphan Hydrobromide / Guaifenesin, 68998-139 — ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, and PHENYLEPHRINE HYDROCHLORIDE, 68998-238 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, and PHENYLEPHRINE HYDROCHLORIDE, 68998-263 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, +1981 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.