Advanced - 75981-370-16 - (Ethyl Alcohol)

Alphabetical Index


Drug Information of Advanced

Product NDC: 75981-370
Proprietary Name: Advanced
Non Proprietary Name: Ethyl Alcohol
Active Ingredient(s): 70    kg/100L & nbsp;   Ethyl Alcohol
Administration Route(s): TOPICAL
Dosage Form(s): GEL
Coding System: National Drug Codes(NDC)

Labeler Information of Advanced

Product NDC: 75981-370
Labeler Name: Geiss, Destin + Dunn, Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part333A
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20120920

Package Information of Advanced

Package NDC: 75981-370-16
Package Description: .059 L in 1 BOTTLE, PLASTIC (75981-370-16)

NDC Information of Advanced

NDC Code 75981-370-16
Proprietary Name Advanced
Package Description .059 L in 1 BOTTLE, PLASTIC (75981-370-16)
Product NDC 75981-370
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ethyl Alcohol
Dosage Form Name GEL
Route Name TOPICAL
Start Marketing Date 20120920
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Geiss, Destin + Dunn, Inc
Substance Name ALCOHOL
Strength Number 70
Strength Unit kg/100L
Pharmaceutical Classes

Complete Information of Advanced


General Information