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equaline nasal

NDC 41163-648 · United Natural Foods, Inc. dba UNFI

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

41163-648-10 — 1 BOTTLE, SPRAY in 1 CARTON (41163-648-10) / 30 mL in 1 BOTTLE, SPRAY

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

37835-527 — acetaminophen, dextromethorphan HBr, Phenylephrine HCl, 37835-651 — PHENYLEPHRINE HYDROCHLORIDE, 41163-035 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 41163-047 — Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 41163-053 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 41163-158 — Ibuprofen, phenylephrine HCl, 41163-188 — mineral oil, petrolatum, phenylephrine HCl, 41163-279 — cocoa butter, phenylephrine HCl, 41163-503 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 41163-603 — acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl, 41163-656 — acetaminophen, dextromethorphan Hbr, Phenylephrine HCl, 41163-664 — Acetaminophen and Phenylephrine HCl, 41163-666 — chlorpheniramine maleate, phenylephrine HCl, 41163-712 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 41163-713 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 41163-737 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin ,Phenylephrine HCL, 41163-738 — dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride, 41163-763 — Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, Phenylephrine HCl, 41163-848 — Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride, 41163-907 — Acetaminophen, Dextromethorphan HBr, 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.