Akin Cough Formula DM

NDC 69822-202 · Southern Sales & Service, Inc.

Generic nameDEXTROMETHORPHAN, GUAIFENESIN

Dosage formLIQUID

RouteORAL

Active ingredient(s)DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN

Strength10; 100 mg/5mL; mg/5mL

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 categoryOTC MONOGRAPH DRUG

Packages

69822-202-04 — 118 mL in 1 BOTTLE (69822-202-04)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

69729-790 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin USP, Phenylephrine Hydrochloride, 69729-802 — Acetaminophen, Dextomethorphan Hydrobromide, Phenylephrine Hydrochloride, 69729-808 — Acetaminohpen, Dextromethorphan Hydrobromide, 69729-809 — Acetaminophen, Dextromethorphan Hydrobromide, 69729-812 — DEXTROMETHORPHAN HYDROBROMIDE and GUAIFENESIN, 69729-816 — Acetaminophen, Dextromethorphan Hydrobromide, 69729-831 — Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride, 69729-833 — Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate, 69732-003 — acetaminophen, guaifenesin, dextromethorphan HBr, phenylephrine HCl, 69822-200 — GUAIFENESIN, 69822-211 — DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, 69822-212 — GUAIFENESIN, 69842-057 — Guaifenesin and Dextromethorphan HBr, 69842-059 — Guaifenesin and Dextromethorphan HBr, 69842-086 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 69842-095 — Guaifenesin 600 mg and Pseudoephedrine HCl 60 mg, 69842-211 — Guaifenesin and Pseudoephedrine HCL, 69842-335 — Guaifenesin, 69842-377 — Benzocaine, 69842-475 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, +2508 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