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NDC 85766-174 · Sportpharm LLC

Generic nameAcetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride

Dosage formTABLET, FILM COATED

RouteORAL

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

Strength325; 10; 100; 5 mg/1; mg/1; mg/1; mg/1

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

85766-174-01 — 50 PACKET in 1 BOX (85766-174-01) / 2 TABLET, FILM COATED in 1 PACKET

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

85722-0001 — DEXTROMETHORPHAN HYDROBROMIDE and GUAIFENESIN, 85722-0002 — DEXTROMETHORPHAN HYDROBROMIDE and GUAIFENESIN, 85766-044 — Acetaminophen, Ibuprofen, 85766-046 — Guaifenesin and Dextromethorphan HBr, 85766-126 — Acetaminophen 500 mg, 85766-140 — mineral oil, petrolatum, phenylephrine HCl, 85766-150 — Guaifenesin and Dextromethorphan HBr, 85766-162 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl ,, 85766-172 — dextromethorphan hydrobromide, guaifenesin, 85766-173 — Acetaminophen, Aspirin, Caffeine, 85766-176 — Guaifenesin and Dextromethorphan Hydrobromide, 85766-177 — Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine succinate, 85766-178 — Phenylephrine HCl, 85766-179 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, 85766-180 — Acetaminophen, Aspirin, Caffeine, 85766-182 — PHENYLEPHRINE HYDROCHLORIDE, 85766-183 — Acetaminophen and Phenylephrine hydrochloride, 85766-223 — Acetaminophen, 85766-250 — Brompheniramine Maleate, Pseudoephedrine Hydrochloride, and Dextromethorphan Hydrobromide, 85786-101 — Acetaminophen, Diphenhydramine Hydrochloride, +5267 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