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Sinus PE plus Allergy

NDC 59779-962 · CVS Pharmacy

Generic nameChlorpheniramine maleate, Phenylephrine HCl
Dosage formTABLET
RouteORAL
Active ingredient(s)CHLORPHENIRAMINE MALEATE, PHENYLEPHRINE HYDROCHLORIDE
Strength4; 10 mg/1; mg/1
Pharmacologic classAdrenergic alpha1-Agonists [MoA], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], alpha-1 Adrenergic Agonist [EPC]
Marketing categoryOTC MONOGRAPH DRUG

Packages

59779-962-08 — 1 BLISTER PACK in 1 CARTON (59779-962-08) / 24 TABLET in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

59779-279 — cocoa butter, phenylephrine HCl, 59779-466 — Acetaminophen and Phenylephrine HCl, 59779-543 — Acetaminophen, Diphenhydramine HCl, Phenylephrine HCl, 59779-603 — acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl, 59779-648 — Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 59779-656 — acetaminophen, dextromethorphan hbr, phenylephrine hcl, 59779-763 — Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, Phenylephrine HCl, 59779-802 — Acetaminophen, Phenylephrine HCl, 59779-838 — Phenylephrine hydrochloride, 59779-944 — glycerin, phenylephrine HCl, pramoxine HCl, white petrolatum, 62011-0443 — Brompheniramine maleate, Phenylephrine HCl, 63102-104 — Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 63102-110 — DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE, 63102-115 — Chlorpheniramine maleate, Phenylephrine hydrochloride, 63102-130 — Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride, 63187-505 — mineral oil, petrolatum, phenylephrine HCl, 63187-652 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 63323-751 — Phenylephrine Hydrochloride, 63629-2303 — Hydrocodone Polistirex and Chlorpheniramine Polistirex, 63629-2304 — Hydrocodone Polistirex and Chlorpheniramine Polistirex, +1679 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.