Handi-Sani - 76063-738-17 - (ALCOHOL)

Alphabetical Index


Drug Information of Handi-Sani

Product NDC: 76063-738
Proprietary Name: Handi-Sani
Non Proprietary Name: ALCOHOL
Active Ingredient(s): .7    mL/mL & nbsp;   ALCOHOL
Administration Route(s): TOPICAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Handi-Sani

Product NDC: 76063-738
Labeler Name: Chromate Industrial Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: part333E
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20110201

Package Information of Handi-Sani

Package NDC: 76063-738-17
Package Description: 532 mL in 1 BOTTLE, PLASTIC (76063-738-17)

NDC Information of Handi-Sani

NDC Code 76063-738-17
Proprietary Name Handi-Sani
Package Description 532 mL in 1 BOTTLE, PLASTIC (76063-738-17)
Product NDC 76063-738
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ALCOHOL
Dosage Form Name LIQUID
Route Name TOPICAL
Start Marketing Date 20110201
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Chromate Industrial Corporation
Substance Name ALCOHOL
Strength Number .7
Strength Unit mL/mL
Pharmaceutical Classes

Complete Information of Handi-Sani


General Information