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GNP Hemorrhoidal

NDC 46122-776 · Amerisourcebergen Drug Corporation

Generic nameHemorrhoidal
Dosage formCREAM
RouteTOPICAL
Active ingredient(s)PETROLATUM, GLYCERIN, PRAMOXINE HYDROCHLORIDE, PHENYLEPHRINE HYDROCHLORIDE
Strength144; 150; 25; 10 mg/g; mg/g; mg/g; mg/g
Pharmacologic classAdrenergic alpha1-Agonists [MoA], Allergens [CS], Cell-mediated Immunity [PE], Glycerol [CS], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Chemical Allergen [EPC], alpha-1 Adrenergic Agonist [EPC]
Marketing categoryOTC MONOGRAPH DRUG

Packages

46122-776-37 — 1 TUBE in 1 CARTON (46122-776-37) / 25.5 g in 1 TUBE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

46122-415 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 46122-418 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 46122-443 — Acetaminophen, Phenylephrine HCl, 46122-660 — ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, and PHENYLEPHRINE HYDROCHLORIDE, 46122-677 — Mineral oil, Petrolatum, Phenylephrine, HCL, 46122-689 — Phenylephrine hydrochloride, 46122-700 — Guaifenesin/phenylephrine, 46122-712 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 46122-714 — White Petrolatum, 46122-745 — Calamine Plus Pramoxine HCl, 46122-777 — Cocoa Butter, Phenylephrine HCl, 47682-001 — ACETAMINOPHEN, PHENYLEPHRINE HYDROCHLORIDE, 47682-017 — PHENYLEPHRINE HYDROCHLORIDE, 47682-047 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl , Guaifenesin, ,, 47682-108 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl ,, 47682-120 — ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, PHENYLEPHRINE HYDROCHLORIDE, 47682-161 — PHENYLEPHRINE HYDROCHLORIDE, 47682-162 — PHENYLEPHRINE HYDROCHLORIDE, 47682-435 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride, 47682-509 — ACETAMINOPHEN, PHENYLEPHRINE HYDROCHLORIDE, +2458 more

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