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HAND SANITIZER - 42584-1001-2 - (ETHYL ALCOHOL)

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Drug Information of HAND SANITIZER

Product NDC: 42584-1001
Proprietary Name: HAND SANITIZER
Non Proprietary Name: ETHYL ALCOHOL
Active Ingredient(s): 62    mL/100mL & nbsp;   ETHYL ALCOHOL
Administration Route(s): TOPICAL
Dosage Form(s): GEL
Coding System: National Drug Codes(NDC)

Labeler Information of HAND SANITIZER

Product NDC: 42584-1001
Labeler Name: HOME DEPOT U.S.A. INC.
Product Type: HUMAN OTC DRUG
FDA Application Number: part333E
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20120214

Package Information of HAND SANITIZER

Package NDC: 42584-1001-2
Package Description: 1 BOTTLE in 1 BLISTER PACK (42584-1001-2) > 53 mL in 1 BOTTLE (42584-1001-1)

NDC Information of HAND SANITIZER

NDC Code 42584-1001-2
Proprietary Name HAND SANITIZER
Package Description 1 BOTTLE in 1 BLISTER PACK (42584-1001-2) > 53 mL in 1 BOTTLE (42584-1001-1)
Product NDC 42584-1001
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ETHYL ALCOHOL
Dosage Form Name GEL
Route Name TOPICAL
Start Marketing Date 20120214
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name HOME DEPOT U.S.A. INC.
Substance Name ALCOHOL
Strength Number 62
Strength Unit mL/100mL
Pharmaceutical Classes

Complete Information of HAND SANITIZER


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