Hanitizer - 67147-221-01 - (ALCOHOL)

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Drug Information of Hanitizer

Product NDC: 67147-221
Proprietary Name: Hanitizer
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 Hanitizer

Product NDC: 67147-221
Labeler Name: Apple Products, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part333E
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20101001

Package Information of Hanitizer

Package NDC: 67147-221-01
Package Description: 1200 mL in 1 CARTRIDGE (67147-221-01)

NDC Information of Hanitizer

NDC Code 67147-221-01
Proprietary Name Hanitizer
Package Description 1200 mL in 1 CARTRIDGE (67147-221-01)
Product NDC 67147-221
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ALCOHOL
Dosage Form Name GEL
Route Name TOPICAL
Start Marketing Date 20101001
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Apple Products, Inc.
Substance Name ALCOHOL
Strength Number .7
Strength Unit mL/mL
Pharmaceutical Classes

Complete Information of Hanitizer


General Information