Cold and Head Congestion Severe

NDC 79481-3572 · Meijer Distribution, Inc.

Generic nameAcetaminophen, Guaifenesin, Phenylephrine HCl

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE

Strength325; 200; 5 mg/1; mg/1; mg/1

Pharmacologic classAdrenergic alpha1-Agonists [MoA], Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], alpha-1 Adrenergic Agonist [EPC]

Marketing categoryOTC MONOGRAPH DRUG

Packages

79481-3572-8 — 2 BLISTER PACK in 1 CARTON (79481-3572-8) / 12 TABLET, FILM COATED in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

79481-0503 — Acetaminophen, Ibuprofen, 79481-0709 — guaifenesin and pseudoephedrine hydrochloride, 79481-0714 — Guaifenesin, 79481-0780 — Acetaminophen, 79481-0807 — Acetaminophen, Dextromethorphan hydrobromide, Phenylephrine hydrochloride, 79481-0808 — Acetaminophen, Dextromethorphan hydrobromide, Doxylamine succinate, 79481-0827 — Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride, 79481-0828 — Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate, 79481-1002 — Guaifenesin and Pseudoephedrine HCl, 79481-1204 — Guaifenesin, 79481-5030 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 79481-5072 — Acetaminophen, Guaifenesin, Phenylephrine HCl, 79481-5100 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, 79481-5196 — Acetaminophen, Guaifenesin, Phenylephrine HCl, 79481-5303 — acetaminophen, dextromethorphan hydrobromide, 79481-5330 — Dextromethorphan HBr, Guaifenesin, 79481-5380 — Acetaminophen, 79481-6170 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 79481-6171 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 79481-6172 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, +4982 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