Pure Gel - 50452-221-17 - (ALCOHOL)

Alphabetical Index


Drug Information of Pure Gel

Product NDC: 50452-221
Proprietary Name: Pure Gel
Non Proprietary Name: ALCOHOL
Active Ingredient(s): .7    mL/mL & nbsp;   ALCOHOL
Administration Route(s): TOPICAL
Dosage Form(s): GEL
Coding System: National Drug Codes(NDC)

Labeler Information of Pure Gel

Product NDC: 50452-221
Labeler Name: Phoenix Research Industries, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part333
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20100201

Package Information of Pure Gel

Package NDC: 50452-221-17
Package Description: 532 mL in 1 BOTTLE, PLASTIC (50452-221-17)

NDC Information of Pure Gel

NDC Code 50452-221-17
Proprietary Name Pure Gel
Package Description 532 mL in 1 BOTTLE, PLASTIC (50452-221-17)
Product NDC 50452-221
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ALCOHOL
Dosage Form Name GEL
Route Name TOPICAL
Start Marketing Date 20100201
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Phoenix Research Industries, Inc.
Substance Name ALCOHOL
Strength Number .7
Strength Unit mL/mL
Pharmaceutical Classes

Complete Information of Pure Gel


General Information