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Cough Relief

NDC 63868-957 · QUALITY CHOICE (Chain Drug Marketing Association)

Generic nameDextromethorphan HBr
Dosage formLIQUID
RouteORAL
Active ingredient(s)DEXTROMETHORPHAN HYDROBROMIDE
Strength15 mg/5mL
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

63868-957-04 — 1 BOTTLE, PLASTIC in 1 BOX (63868-957-04) / 118 mL in 1 BOTTLE, PLASTIC

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

63868-589 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 63868-736 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 63868-737 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, 63868-745 — dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, 63868-746 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 63868-753 — Dextromethorphan Hydrobromide / Guaifenesin, 63868-771 — GUAIFENESIN and DEXTROMETHORPHAN HYDROBROMIDE, 63868-868 — Dextromethorphan HBr, Guaifenesin, 63868-869 — Dextromethorphan HBr, Guaifenesin, 63868-870 — Guaifenesin, Dextromethorphan HBr, 63941-263 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 63941-274 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 63941-309 — Dextromethorphan HBr, 63941-343 — Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, 63941-344 — Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, 63941-382 — Dextromethorphan HBr, Guaifenesin, Phenylephrine, 63941-385 — Dextromethorphan HBr, Guaifenesin, 63941-399 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 63941-455 — Dextromethorphan HBr, 63941-466 — Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride, +1967 more

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