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Mucus Relief DM Extended Release Caplets

NDC 17856-1162 · ATLANTIC BIOLOGICALS CORP.

Generic nameGuaifenesin, Dextromethorphan HBr
Dosage formTABLET, EXTENDED RELEASE
RouteORAL
Active ingredient(s)GUAIFENESIN, DEXTROMETHORPHAN HYDROBROMIDE
Strength30; 600 mg/1; mg/1
Pharmacologic classDecreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA]
Marketing categoryANDA

Packages

17856-1162-1 — 100 BLISTER PACK in 1 CARTON (17856-1162-1) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

12539-555 — Guaifenesin, Dextromethorphan HBr, 12539-779 — Dextromethorphan HBr, Chlorpheniramine Maleate, Phenylephrine HCl, 12830-816 — Dexbrompheniramine Maleate, Dextromethorphan Hydrobromide, Pseudoephedrine Hydrochloride, 16103-379 — GUAIFENESIN, 16103-381 — GUAIFENESIN 400mg and DEXTROMETHORPHAN HBR 20MG, 17714-150 — Guaifenesin and Dextromethorphan HBr, 17714-152 — Guaifenesin 400 mg, 17856-0008 — Guaifenesin, 17856-0155 — Promethazine Hydrochloride and Dextromethorphan Hydrobromide Oral Solution, 17856-1126 — Dextromethorphan HBr, Guaifenesin, 17856-4024 — Promethazine Hydrochloride and Dextromethorphan Hydrobromide, 17856-6312 — dextromethorphan polistirex, 21130-012 — dextromethorphan polistirex, 21130-036 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 21130-044 — Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate, 21130-091 — acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl, 21130-129 — Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, Phenylephrine HCl, 21130-162 — Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride, 21130-179 — Guaifenesin, 21130-343 — Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate, +2508 more

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