Skip to main content

Good Sense Nasal Four

NDC 0113-0648 · L. Perrigo Company

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

0113-0648-10 — 1 BOTTLE, SPRAY in 1 CARTON (0113-0648-10) / 29.6 mL in 1 BOTTLE, SPRAY

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0067-8132 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 0067-8136 — acetaminophen, dextromethorphan HBr, phenylephrine HCl, 0067-8137 — acetaminophen, diphenhydramine HCl, phenylephrine HCl, 0067-8145 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 0067-8211 — ACETAMINOPHEN, DEXTROMETHORPHAN HBr, PHENYLEPHRINE HCl, 0067-8212 — ACETAMINOPHEN, DIPHENHYDRAMINE HCl, PHENYLEPHRINE HCl, 0113-0019 — Acetaminophen, dextromethorphan HBr, doxylamine succinate, phenylephrine HCl, 0113-0188 — mineral oil, petrolatum, phenylephrine HCl, 0113-0279 — cocoa butter, phenylephrine HCl, 0113-0603 — acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl, 0113-0656 — acetaminophen, dextromethorphan Hbr, Phenylephrine HCl, 0113-0763 — Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, Phenylephrine HCl, 0113-0944 — glycerin, phenylephrine HCl, pramoxine HCl, white petrolatum, 0113-0987 — Brompheniramine maleate, Dextromethorphan HBr, Phenylephrine HCl, 0113-0994 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 0113-2299 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, 0113-2501 — acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, phenylephrine hydrochloride, 0113-4500 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, 0135-0578 — acetaminophen, chlorpheniramine maleate, phenylephrine hcl, 0135-0607 — acetaminophen and phenyleprine 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.