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ETHYL ALCOHOL - 21749-967-89 - (ALCOHOL)

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Drug Information of ETHYL ALCOHOL

Product NDC: 21749-967
Proprietary Name: ETHYL ALCOHOL
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 ETHYL ALCOHOL

Product NDC: 21749-967
Labeler Name: GOJO Industries, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part333
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20100526

Package Information of ETHYL ALCOHOL

Package NDC: 21749-967-89
Package Description: 1200 mL in 1 BOTTLE (21749-967-89)

NDC Information of ETHYL ALCOHOL

NDC Code 21749-967-89
Proprietary Name ETHYL ALCOHOL
Package Description 1200 mL in 1 BOTTLE (21749-967-89)
Product NDC 21749-967
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ALCOHOL
Dosage Form Name GEL
Route Name TOPICAL
Start Marketing Date 20100526
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name GOJO Industries, Inc.
Substance Name ALCOHOL
Strength Number .7
Strength Unit mL/mL
Pharmaceutical Classes

Complete Information of ETHYL ALCOHOL


General Information