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hemorrhoidal - 37808-944-24 - (glycerin, phenylephrine HCl, pramoxine HCl, white petrolatum)

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Drug Information of hemorrhoidal

Product NDC: 37808-944
Proprietary Name: hemorrhoidal
Non Proprietary Name: glycerin, phenylephrine HCl, pramoxine HCl, white petrolatum
Active Ingredient(s): 14.4; 15; .25; 1    g/100g; g/100g; g/100g; g/100g & nbsp;   glycerin, phenylephrine HCl, pramoxine HCl, white petrolatum
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of hemorrhoidal

Product NDC: 37808-944
Labeler Name: H E B
Product Type: HUMAN OTC DRUG
FDA Application Number: part346
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20121025

Package Information of hemorrhoidal

Package NDC: 37808-944-24
Package Description: 1 TUBE in 1 CARTON (37808-944-24) > 51 g in 1 TUBE

NDC Information of hemorrhoidal

NDC Code 37808-944-24
Proprietary Name hemorrhoidal
Package Description 1 TUBE in 1 CARTON (37808-944-24) > 51 g in 1 TUBE
Product NDC 37808-944
Product Type Name HUMAN OTC DRUG
Non Proprietary Name glycerin, phenylephrine HCl, pramoxine HCl, white petrolatum
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20121025
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name H E B
Substance Name GLYCERIN; PETROLATUM; PHENYLEPHRINE HYDROCHLORIDE; PRAMOXINE HYDROCHLORIDE
Strength Number 14.4; 15; .25; 1
Strength Unit g/100g; g/100g; g/100g; g/100g
Pharmaceutical Classes

Complete Information of hemorrhoidal


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