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Antibacterial - 49794-010-99 - (Ethyl Alcohol)

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Drug Information of Antibacterial

Product NDC: 49794-010
Proprietary Name: Antibacterial
Non Proprietary Name: Ethyl Alcohol
Active Ingredient(s): 620    g/L & nbsp;   Ethyl Alcohol
Administration Route(s): TOPICAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Antibacterial

Product NDC: 49794-010
Labeler Name: Continental Manufacturing Chemist, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part333A
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20110901

Package Information of Antibacterial

Package NDC: 49794-010-99
Package Description: 1100 L in 1 CONTAINER (49794-010-99)

NDC Information of Antibacterial

NDC Code 49794-010-99
Proprietary Name Antibacterial
Package Description 1100 L in 1 CONTAINER (49794-010-99)
Product NDC 49794-010
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ethyl Alcohol
Dosage Form Name LIQUID
Route Name TOPICAL
Start Marketing Date 20110901
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Continental Manufacturing Chemist, Inc.
Substance Name ALCOHOL
Strength Number 620
Strength Unit g/L
Pharmaceutical Classes

Complete Information of Antibacterial


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