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NASAL and SINUS DECONGESTANT

NDC 73598-1262 · JHK Inc dba American Safety & First Aid

Generic namePHENYLEPHRINE HYDROCHLORIDE
Dosage formTABLET
RouteORAL
Active ingredient(s)PHENYLEPHRINE HYDROCHLORIDE
Strength5 mg/1
Pharmacologic classAdrenergic alpha1-Agonists [MoA], alpha-1 Adrenergic Agonist [EPC]
Marketing categoryOTC MONOGRAPH DRUG

Packages

73598-1262-1 — 50 PACKET in 1 BOX (73598-1262-1) / 2 TABLET in 1 PACKET

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

72854-203 — Acetaminophen, Dextromethorphan Hydrobromide, and Phenylephrine Hydrochloride, 72854-234 — Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride, and Triprolidine Hydrochloride, 72854-240 — Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride, and Triprolidine Hydrochloride, 72976-018 — Phenylephrine HCl, 73057-389 — GUAIFENESIN 400mg and PHENYLEPHRINE HCL 10MG, 73097-011 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE, 73097-014 — ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE, 73408-835 — Acetaminophen, Dextromethorphan HBr, Phenylephrine, Guaifenesin, ,, 73408-990 — phenylephrine hydrochloride, 73581-204 — PHENYLPHRINE HCL, 73598-1264 — PHENYLEPHRINE HYDROCHLORIDE, 73598-1342 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride, 75907-129 — PHENYLEPHRINE HYDROCHLORIDE, 75907-130 — PHENYLEPHRINE HYDROCHLORIDE, 75907-324 — PHENYLEPHRINE HYDROCHLORIDE, 76095-010 — Acetaminophen Chlorpheniramine Maleate Phenylepherine Hydrochloride, 76095-011 — Acetaminophen Chlorpheniramine Maleate Phenylepherine Hydrochloride, 76117-001 — CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE, 76162-000 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride, 76162-040 — 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.