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Good Sense Hemorrhoidal

NDC 0113-0188 · L. Perrigo Company

Generic namemineral oil, petrolatum, phenylephrine HCl
Dosage formOINTMENT
RouteRECTAL
Active ingredient(s)MINERAL OIL, PETROLATUM, PHENYLEPHRINE HYDROCHLORIDE
Strength14; 74.9; .25 g/100g; g/100g; g/100g
Pharmacologic classAdrenergic alpha1-Agonists [MoA], alpha-1 Adrenergic Agonist [EPC]
Marketing categoryOTC MONOGRAPH DRUG

Packages

0113-0188-16 — 1 TUBE in 1 CARTON (0113-0188-16) / 57 g in 1 TUBE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 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, 0113-0279 — cocoa butter, phenylephrine HCl, 0113-0603 — acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl, 0113-0648 — Phenylephrine hydrochloride, 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, +1997 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.