Dermadrox - 54162-221-01 - (Aluminum Hydroxide)

Alphabetical Index


Drug Information of Dermadrox

Product NDC: 54162-221
Proprietary Name: Dermadrox
Non Proprietary Name: Aluminum Hydroxide
Active Ingredient(s): 1.2    g/100g & nbsp;   Aluminum Hydroxide
Administration Route(s): TOPICAL
Dosage Form(s): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of Dermadrox

Product NDC: 54162-221
Labeler Name: GERITREX CORP
Product Type: HUMAN OTC DRUG
FDA Application Number: part346
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20130130

Package Information of Dermadrox

Package NDC: 54162-221-01
Package Description: 113 g in 1 TUBE (54162-221-01)

NDC Information of Dermadrox

NDC Code 54162-221-01
Proprietary Name Dermadrox
Package Description 113 g in 1 TUBE (54162-221-01)
Product NDC 54162-221
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Aluminum Hydroxide
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 20130130
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name GERITREX CORP
Substance Name ALUMINUM HYDROXIDE
Strength Number 1.2
Strength Unit g/100g
Pharmaceutical Classes

Complete Information of Dermadrox


General Information