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QUALITY CHOICE

NDC 83324-215 · CHAIN DRUG MARKETING ASSOCIATION

Generic namePhenylephrine Hydrochloride
Dosage formSOLUTION/ DROPS
RouteNASAL
Active ingredient(s)PHENYLEPHRINE HYDROCHLORIDE
Strength1 g/100mL
Pharmacologic classAdrenergic alpha1-Agonists [MoA], alpha-1 Adrenergic Agonist [EPC]
Marketing categoryOTC MONOGRAPH DRUG

Packages

83324-215-01 — 1 BOTTLE, DROPPER in 1 CARTON (83324-215-01) / 30 mL in 1 BOTTLE, DROPPER

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

83324-114 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 83324-115 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 83324-143 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 83324-144 — Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 83324-145 — Acetaminophen Dextromethorphan HBr Phenylephrine HCl, 83324-155 — Dextromethorphan HBr Guaifenesin Phenylephrine HCl, 83324-156 — Brompheniramine maleate, Phenylephrine HCl, 83324-162 — Acetaminophen, Dextromethorphan hydrobromide, Guaifenesin, Phenylephrine hydrochloride, 83324-167 — Acetaminophen Dextromethorphan HBr Phenylephrine HCl, 83324-168 — Acetaminophen Dextromethorphan HBr Phenylephrine HCl, 83324-224 — Acetaminophen, Dextromethorphan hydrobromide, Doxylamine succinate, Phenylephrine hydrochloride, 83324-330 — Glycerin, Phenylephine HCI, Pramoxine HCI, Petrolatum, 83586-004 — Acetaminophen, Diphenhydramine Hydrochloride, and Phenylephrine Hydrochloride, 83586-010 — PHENYLEPHRINE HYDROCHLORIDE, 83586-160 — PHENYLEPHRINE HYDROCHLORIDE, 84000-502 — COCOA BUTTER, GLYCERIN, LIDOCAINE, PETROLATUM, PHENYLEPHRINE HYDROCHLORIDE, 84126-315 — Acetaminophen, Dextromethorphan Hydrobromide, and Phenylephrine Hydrochloride, 84269-2546 — ACETAMINOPHEN, PHENYLEPHRINE HYDROCHLORIDE, 84269-2556 — PHENYLEPHRINE HYDROCHLORIDE, ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, 84308-161 — Glycerin, Lidocaine, Petrolatum, Phenylephrine HCl, +1522 more

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