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NDC 0924-0133 · Acme United Corporation

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

0924-0133-01 — 50 PACKET in 1 CARTON (0924-0133-01) / 1 TABLET, FILM COATED in 1 PACKET (0924-0133-00)

0924-0133-03 — 10 PACKET in 1 CARTON (0924-0133-03) / 1 TABLET, FILM COATED in 1 PACKET (0924-0133-00)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0781-3458 — Phenylephrine Hydrochloride, 0781-3466 — Phenylephrine Hydrochloride, 0781-9226 — Phenylephrine Hydrochloride, 0781-9227 — Phenylephrine Hydrochloride, 0781-9228 — Phenylephrine Hydrochloride, 0904-5786 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 0904-6463 — Brompheniramine maleate, Dextromethorphan HBr, Phenylephrine HCl, 0904-6537 — Dextromethorphan HBr, Guaifenesin, Phenylephrine, 0904-6995 — ACETAMINOHPEN, DEXTROMETHORPHAN HBr, PHENYLEPHRINE HCL, 0924-0091 — Acetaminophen, Chlorpheniramine Maleate, Phenylephrine Hydrochloride, 0924-0142 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride, 10157-2126 — WHITE PETROLATUM, GLYCERIN, PRAMOXINE HYDROCHLORIDE, and PHENYLEPHRINE HYDROCHLORIDE, 11673-113 — Acetaminophen, Diphenhydramine hydrochloride, and Phenylephrine hydrochloride, 11673-322 — Acetaminophen, Dextromethrophan, Doxylamine succinate, Phenylephrine HCl, 11673-337 — Dextromethorphan HBr, Guaifenesin, Phenylephrine HCI, 11673-347 — acetaminophen, dextromethorphan HBr, guaifenesin, phenylephrine HCl, 11673-410 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 11673-738 — dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride, 11673-765 — Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine HCl, 11673-773 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, +1523 more

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