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ANTIBACTERIAL - 49738-294-50 - (TRICLOSAN)

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Drug Information of ANTIBACTERIAL

Product NDC: 49738-294
Proprietary Name: ANTIBACTERIAL
Non Proprietary Name: TRICLOSAN
Active Ingredient(s): .15    L/100L & nbsp;   TRICLOSAN
Administration Route(s): TOPICAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of ANTIBACTERIAL

Product NDC: 49738-294
Labeler Name: KMART CORPORATION
Product Type: HUMAN OTC DRUG
FDA Application Number: part333E
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20110601

Package Information of ANTIBACTERIAL

Package NDC: 49738-294-50
Package Description: 4 L in 1 BOTTLE (49738-294-50)

NDC Information of ANTIBACTERIAL

NDC Code 49738-294-50
Proprietary Name ANTIBACTERIAL
Package Description 4 L in 1 BOTTLE (49738-294-50)
Product NDC 49738-294
Product Type Name HUMAN OTC DRUG
Non Proprietary Name TRICLOSAN
Dosage Form Name LIQUID
Route Name TOPICAL
Start Marketing Date 20110601
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name KMART CORPORATION
Substance Name TRICLOSAN
Strength Number .15
Strength Unit L/100L
Pharmaceutical Classes

Complete Information of ANTIBACTERIAL


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