Skip to main content

ValuMeds Nasal Decongestant Phenylephrine HCl

NDC 82725-1111 · Cabinet Health P.B.C.

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

Packages

82725-1111-1 — 300 TABLET in 1 BOTTLE (82725-1111-1)

82725-1111-2 — 100 TABLET in 1 BOTTLE (82725-1111-2)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

82433-946 — LIDOCAINE, PHENYLEPHRINE HYDROCHLORIDE, 82442-025 — 14.4% Glycerin, 0.25% Phenylephrine HCL, 1% Pramoxine HCL, 15% Petrolatum, 82442-060 — Phenylephrine hydrochloride, 82442-119 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, 82442-645 — brompheniramine maleate, dextromethorphan HBr, phenylephrine HCl, 82442-694 — Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride, 82673-103 — Diphenhydramine HCl, Phenylephrine HCl, 82688-001 — Acetaminophen Phenylephrine HCl Chlorpheniramine Maleate, 82706-020 — Acetaminophen, Guaifenesin, Phenylephrine Hydrocloride, 82706-025 — Acetaminophen, Phenylephrine Hydrochloride, 83004-039 — LIDOCAINE, PHENYLEPHRINE HYDROCHLORIDE, 83059-0023 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 83059-0044 — Acetaminophen 325 mg, Diphenhydramine HCl 12.5 mg, Phenylephrine HCl 5 mg, 83059-0045 — Acetaminophen 325 mg, Diphenhydramine HCl 12.5 mg, Phenylephrine HCl 5 mg, 83059-0057 — Acetaminophen, Guaifenesin, Phenylephrine, 83059-0071 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 83059-0106 — Acetaminophen 325 mg, Diphenhydramine HCl 12.5 mg, Phenylephrine HCl 5 mg, 83059-0107 — Acetaminophen, Guaifenesin, Phenylephrine, 83059-0113 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 83059-0114 — Acetaminophen, Dextromethorphan HBr, 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.