Sani - 50522-221-03 - (ALCOHOL)

Alphabetical Index


Drug Information of Sani

Product NDC: 50522-221
Proprietary Name: Sani
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 Sani

Product NDC: 50522-221
Labeler Name: AIS Specialty Products, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part333E
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20120524

Package Information of Sani

Package NDC: 50522-221-03
Package Description: 350 mL in 1 CARTRIDGE (50522-221-03)

NDC Information of Sani

NDC Code 50522-221-03
Proprietary Name Sani
Package Description 350 mL in 1 CARTRIDGE (50522-221-03)
Product NDC 50522-221
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ALCOHOL
Dosage Form Name GEL
Route Name TOPICAL
Start Marketing Date 20120524
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name AIS Specialty Products, Inc.
Substance Name ALCOHOL
Strength Number .7
Strength Unit mL/mL
Pharmaceutical Classes

Complete Information of Sani


General Information