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Head Congestion and Flu Severe

NDC 11822-5462 · Rite Aid Corporation

Generic nameAcetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE
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

11822-5462-9 — 2 BLISTER PACK in 1 CARTON (11822-5462-9) / 10 TABLET, FILM COATED in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

11822-4484 — Acetaminophen, 11822-4530 — Phenylephrine HCl, 11822-4669 — Acetaminophen, Phenylephrine HCl, 11822-5019 — Acetaminophen, 11822-5022 — Acetaminophen and Phenylephrine HCl, 11822-5031 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 11822-5050 — Dextromethorphan Hydrobromide Guaifenesin, 11822-5091 — Acetaminophen, 11822-5160 — Acetaminophen, Guaifenesin, Phenylephrine HCl, 11822-5311 — Acetaminophen, 11822-5777 — Acetaminophen, Ibuprofen, 11822-5832 — Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate, 11822-6005 — Dextromethorphan Hydrobromide, Doxylamine Succinate, 11822-6179 — ACETAMINOPHEN, DEXTROMETHORPHAN HBr, GUAIFENESIN, PHENYLEPHRINE HCl, 11822-6790 — acetaminophen, pamabrom, pyrilamine maleate, 11822-7340 — Guaifenesin, Dextromethorphan HBr, 11822-7380 — Acetaminophen, Chlorpheniramine maleate, Dextromethorphan HBr, 11822-7399 — Guaifenesin and Pseudoephedrine HCL, 11822-8003 — Acetaminophen, 11822-8791 — Diphenhydramine Hydrochloride and Acetaminophen, +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