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ANTIBACTERIAL FOAMING HAND SP - 59779-169-08 - (TRICLOSAN)

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Drug Information of ANTIBACTERIAL FOAMING HAND SP

Product NDC: 59779-169
Proprietary Name: ANTIBACTERIAL FOAMING HAND SP
Non Proprietary Name: TRICLOSAN
Active Ingredient(s): .6    mL/100mL & nbsp;   TRICLOSAN
Administration Route(s): TOPICAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of ANTIBACTERIAL FOAMING HAND SP

Product NDC: 59779-169
Labeler Name: CVS PHARMACY
Product Type: HUMAN OTC DRUG
FDA Application Number: part333E
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20110203

Package Information of ANTIBACTERIAL FOAMING HAND SP

Package NDC: 59779-169-08
Package Description: 221 mL in 1 BOTTLE, PUMP (59779-169-08)

NDC Information of ANTIBACTERIAL FOAMING HAND SP

NDC Code 59779-169-08
Proprietary Name ANTIBACTERIAL FOAMING HAND SP
Package Description 221 mL in 1 BOTTLE, PUMP (59779-169-08)
Product NDC 59779-169
Product Type Name HUMAN OTC DRUG
Non Proprietary Name TRICLOSAN
Dosage Form Name LIQUID
Route Name TOPICAL
Start Marketing Date 20110203
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name CVS PHARMACY
Substance Name TRICLOSAN
Strength Number .6
Strength Unit mL/100mL
Pharmaceutical Classes

Complete Information of ANTIBACTERIAL FOAMING HAND SP


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