VANACOF DM

NDC 58809-555 · GM Pharmaceuticals, INC

Generic nameDEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE

Dosage formLIQUID

RouteORAL

Active ingredient(s)DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE

Strength18; 200; 10 mg/15mL; mg/15mL; mg/15mL

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

58809-555-08 — 240 mL in 1 BOTTLE (58809-555-08)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

58657-504 — Guaifenesin and Dextromethorphan Hydrobromide, 58657-505 — Guaifenesin and Dextromethorphan Hydrobromide, 58657-508 — Guaifenesin, 58657-509 — Guaifenesin, 58657-851 — Phenylephrine Hydrochloride, 58657-852 — Phenylephrine Hydrochloride, 58657-853 — Phenylephrine Hydrochloride, 58809-187 — Dextromethorphan HBr, Guaifenesin, 58809-217 — Choline Salicylate, Dextromethorphan Hydrobromide, Guaifenesin, 58809-218 — Choline Salicylate,Guaifenesin, 58933-550 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 58933-551 — Acetaminophen, Diphenhydramine HCl, Phenylephrine HCl, 58933-552 — Acetaminophen, Dextromethorphan HBr, 59148-053 — dextromethorphan hydrobromide and quinidine sulfate, 59450-046 — Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride, 59450-047 — Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate, 59640-010 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride, 59640-100 — dextromethorphan hydrobromide, guaifenesin, 59640-200 — brompheniramine maleate, dextromethorphan hydrobromide, 59640-300 — guaifenesin, pseudoephedrine hydrochloride, +3082 more

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

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels