Skip to main content

Nasal

NDC 79481-0101 · Meijer, Inc.

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

Packages

79481-0101-0 — 1 BOTTLE in 1 CARTON (79481-0101-0) / 30 mL in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

76162-912 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 76162-913 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, Phenylephrine HCl, 76281-304 — ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL, 76281-306 — ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL, 76281-504 — DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE, 76281-506 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 76281-515 — ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCl, 76281-517 — Dextromethorphan HBr, GUaifenesin, Phenylephrine HCL, 76281-519 — ACETAMINOPHEN, DEXTROMETHORPHAN HBr, GUAIFENESIN, PHENYLEPHRINE HCL, 76281-604 — ACETAMINOPHEN, DEXTROMETHORPHAN HBr, PHENYLEPHRINE HCl, 79481-0807 — Acetaminophen, Dextromethorphan hydrobromide, Phenylephrine hydrochloride, 79481-0827 — Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride, 79481-3572 — Acetaminophen, Guaifenesin, Phenylephrine HCl, 79481-5030 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 79481-5072 — Acetaminophen, Guaifenesin, Phenylephrine HCl, 79481-5100 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, 79481-5196 — Acetaminophen, Guaifenesin, Phenylephrine HCl, 79481-6170 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 79481-6171 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 79481-6172 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, 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.