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CVS Childrens Cold and Allergy

NDC 69842-639 · CVS PHARMACY, INC.

Generic nameBrompheniramine maleate, Phenylephrine HCl
Dosage formLIQUID
RouteORAL
Active ingredient(s)BROMPHENIRAMINE MALEATE, PHENYLEPHRINE HYDROCHLORIDE
Strength2; 5 mg/10mL; mg/10mL
Pharmacologic classAdrenergic alpha1-Agonists [MoA], alpha-1 Adrenergic Agonist [EPC]
Marketing categoryOTC MONOGRAPH DRUG

Packages

69842-639-04 — 1 BOTTLE in 1 CARTON (69842-639-04) / 118 mL in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

69732-003 — acetaminophen, guaifenesin, dextromethorphan HBr, phenylephrine HCl, 69805-400 — Lidocaine 5%, Phenylephrine Hydrochloride 0.25%, 69842-443 — Phenylephrine Hydrochloride, 69842-475 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 69842-487 — Childrens Stuffy Nose and Cold, 69842-503 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 69842-505 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 69842-566 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin ,Phenylephrine HCL, 69842-570 — Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 69842-616 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE, 69842-648 — Phenylephrine hydrochloride, 69842-651 — Acetaminophen, Guaifenesin, Phenylephrine HCl, 69842-717 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 69842-723 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, 69842-756 — Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 69842-767 — dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride, 69842-779 — Brompheniramine maleate, Phenylephrine HCl, 69842-785 — Cocoa Butter, Phenylephrine HCl, 69842-789 — ACETAMINOPHEN,DEXTROMETHORPHAN HYDROBROMIDE,GUAIFENESIN,PHENYLEPHRINE HYDROCHLORIDE, 69842-796 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, +1566 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