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ACTIDOM DMX

NDC 63102-110 · ACTIPHARMA, LLC

Generic nameDEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE
Dosage formSOLUTION
RouteORAL
Active ingredient(s)DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE
Strength30; 200; 10 mg/5mL; mg/5mL; mg/5mL
Pharmacologic classAdrenergic alpha1-Agonists [MoA], Decreased 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], alpha-1 Adrenergic Agonist [EPC]
Marketing categoryOTC MONOGRAPH DRUG

Packages

63102-110-16 — 474 mL in 1 BOTTLE, PLASTIC (63102-110-16)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

62207-569 — GUAIFENESIN, 62207-570 — GUAIFENESIN, 62207-827 — Guaifenesin and Pseudoephedrine HCl, 62207-828 — Guaifenesin and Pseudoephedrine HCl, 62207-839 — GUAIFENESIN, 62207-840 — GUAIFENESIN, 62559-758 — Promethazine Hydrochloride and Dextromethorphan Hydrobromide, 63102-101 — Dextromethorphan HBr,Guaifenesin,Pseudoephedrine HCl, 63102-102 — Dextromethorphan HBr,Guaifenesin,Pseudoephedrine HCl, 63102-104 — Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 63102-115 — Chlorpheniramine maleate, Phenylephrine hydrochloride, 63102-120 — Dextromethorphan Hydrobromide, Guaifenesin, Pseudoephedrine Hydrochloride, 63102-130 — Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride, 63102-140 — Dextromethorphan Hydrobromide, Guaifenesin, 63187-505 — mineral oil, petrolatum, phenylephrine HCl, 63187-652 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 63187-664 — Brompheniramine Maleate, Pseudoephedrine Hydrochloride and Dextromethorphan Hydrobromide, 63187-930 — Brompheniramine Maleate, Pseudoephedrine Hydrochloride, and Dextromethorphan Hydrobromide, 63187-954 — Guaifenesin, 63304-106 — Guaifenesin and Dextromethorphan HBr, +3082 more

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