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Sinus Congestion

NDC 50844-493 · L.N.K. International, Inc.

Generic namePhenylephrine HCl
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)PHENYLEPHRINE HYDROCHLORIDE
Strength10 mg/1
Pharmacologic classAdrenergic alpha1-Agonists [MoA], alpha-1 Adrenergic Agonist [EPC]
Marketing categoryOTC MONOGRAPH DRUG

Packages

50844-493-07 — 2 BLISTER PACK in 1 CARTON (50844-493-07) / 18 TABLET, FILM COATED in 1 BLISTER PACK

50844-493-08 — 1 BLISTER PACK in 1 CARTON (50844-493-08) / 24 TABLET, FILM COATED in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50804-256 — Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 50804-274 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 50804-317 — Glycerin, Lidocaine, Petrolatum, Phenylephrine HCl, 50804-503 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 50804-672 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 50804-805 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 50844-004 — Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 50844-251 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 50844-455 — Acetaminophen, Chlorpheniramine maleate, Phenylephrine HCl, 50844-467 — Acetaminophen, Phenylephrine HCl, 50844-572 — Acetaminophen, Guaifenesin, Phenylephrine HCl, 50844-640 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 50844-677 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, Phenylephrine HCl, 50991-132 — Dextromethorphan HBr, Phenylephrine HCl, Pyrilamine Maleate, 50991-444 — Dextromethorphan HBr, Pheniramine Maleate, Phenylephrine HCl, 50991-626 — Doxylamine Succinate and Phenylephrine Hydrochloride, 50991-736 — Guaifenesin and Phenylephrine HCl, 50991-740 — Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride, 50991-776 — Pheniramine Maleate, Phenylephrine HCl, 50991-788 — Dexbrompheniramine Maleate, Phenylephrine Hydrochloride, +1523 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.