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CVS Dex-Dox Kids Nighttime Cough Suppressant

NDC 51316-081 · CVS

Generic nameDextromethorphan HBr
Dosage formCHEWABLE GEL
RouteORAL
Active ingredient(s)DOXYLAMINE SUCCINATE, DEXTROMETHORPHAN HYDROBROMIDE
Strength10; 6.25 mg/1; mg/1
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

51316-081-16 — 16 CHEWABLE GEL in 1 BOTTLE (51316-081-16)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

51013-174 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, 51013-175 — Acetaminophen, Phenylephrine hydrochloride, Doxylamine succinate, Dextromethorphan hydrobromide, 51013-666 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, 51013-667 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, 51013-668 — acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, 51316-009 — Guaifenesin and Dextromethorphan HBR, 51316-060 — Guaifenesin and Dextromethorphan HBr, 51316-062 — Dextromethorphan Hydrobromide, Doxylamine succinate, 51316-065 — Guaifenesin and Dextromethorphan HBr, 51316-080 — Dextromethorphan HBr, 51316-082 — dextromethorphan hydrobromide, guaifenesin, 51316-089 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, 51316-179 — acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, phenylephrine hydrochloride, 51316-189 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, 51316-263 — dextromethorphan polistirex, 51316-293 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, 51316-304 — Dextromethorphan HBr, Guaifenesin, 51316-305 — Dextromethorphan HBr, Guaifenesin, 51316-310 — Dextromethorphan HBr, Guaifenesin, 51316-323 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride, +2034 more

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