Severe Cold

NDC 69842-505 · CVS Pharmacy

Generic nameAcetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl

Dosage formCAPSULE

RouteORAL

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

Strength325; 10; 200; 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

69842-505-16 — 16 BLISTER PACK in 1 CARTON (69842-505-16) / 1 CAPSULE in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

69842-445 — Acetaminophen, 69842-448 — Diphenhydramine Hydrochloride and Acetaminophen, 69842-449 — Acetaminophen, 69842-450 — Acetaminophen, 69842-465 — Acetaminophen, 69842-475 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 69842-484 — Acetaminophen, 69842-487 — Childrens Stuffy Nose and Cold, 69842-491 — Acetaminophen, 69842-503 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 69842-513 — dextromethorphan hydrobromide, guaifenesin, 69842-541 — Acetaminophen, Aspirin, Caffeine, 69842-566 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin ,Phenylephrine HCL, 69842-570 — Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 69842-572 — ACETAMINOPHEN, DIPHENHYDRAMINE HCL, 69842-577 — DEXTROMETHORPHAN HYDROBROMIDE AND GUAIFENESIN, 69842-586 — Acetaminophen, Aspirin, Caffeine, 69842-591 — Acetaminophen 250mg Aspirin 250mg Caffeine 65mg, 69842-592 — Acetaminophen 250mg Aspirin 250mg Caffeine 65mg, 69842-616 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE 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