Skip to main content

4 Way

NDC 0067-2086 · Haleon US Holdings LLC

Generic namePhenylephrine hydrochloride
Dosage formSPRAY
RouteNASAL
Active ingredient(s)PHENYLEPHRINE HYDROCHLORIDE
Strength10 mg/mL
Pharmacologic classAdrenergic alpha1-Agonists [MoA], alpha-1 Adrenergic Agonist [EPC]
Marketing categoryOTC MONOGRAPH DRUG

Packages

0067-2086-01 — 1 BOTTLE, SPRAY in 1 CARTON (0067-2086-01) / 29.6 mL in 1 BOTTLE, SPRAY

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0031-8716 — dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride, 0031-8742 — dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride, 0031-8751 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, 0031-8752 — acetaminophen, diphenhydramine hydrochloride, phenylephrine hydrochloride, 0065-0343 — Phenylephrine Hydrochloride, 0065-0349 — Phenylephrine Hydrochloride, 0065-0359 — cyclopentolate hydrochloride and phenylephrine hydrochloride, 0067-6094 — ACETAMINOPHEN, DEXTROMETHORPHAN, PHENYLEPHRINE, 0067-6095 — ACETAMINOPHEN, DIPHENHYDRAMINE HCL, PHENYLEPHRINE HCL, 0067-6426 — ACETAMINOPHEN, DEXTROMETHORPHAN HBr, PHENYLEPHRINE HCl, 0067-6800 — Acetaminophen, Dextromethorphan HBr, Phenylephrine Hydrochloride, 0067-6801 — Acetaminophen, Diphenhydramine Hydrochloride, Phenylephrine Hydrochloride, 0067-6802 — ACETAMINOPHEN, DEXTROMETHORPHAN HBr, PHENYLEPHRINE HCl, 0067-6803 — ACETAMINOPHEN, DIPHENHYDRAMINE HCl, PHENYLEPHRINE HCl, 0067-7917 — ACETAMINOPHEN, DEXTROMETHORPHAN, PHENYLEPHRINE, 0067-7918 — ACETAMINOPHEN, DIPHENHYDRAMINE HCL, PHENYLEPHRINE HCL, 0067-8127 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 0067-8129 — Acetaminophen, Diphenhydramine HCl, Phenylephrine HCl, 0067-8132 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 0067-8136 — 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.