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ANTIBACTERIAL FOAMING - 36800-169-08 - (TRICLOSAN)

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Drug Information of ANTIBACTERIAL FOAMING

Product NDC: 36800-169
Proprietary Name: ANTIBACTERIAL FOAMING
Non Proprietary Name: TRICLOSAN
Active Ingredient(s): .46    mL/100mL & nbsp;   TRICLOSAN
Administration Route(s): TOPICAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of ANTIBACTERIAL FOAMING

Product NDC: 36800-169
Labeler Name: TOPCO ASSOCIATES LLC
Product Type: HUMAN OTC DRUG
FDA Application Number: part333E
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20111101

Package Information of ANTIBACTERIAL FOAMING

Package NDC: 36800-169-08
Package Description: 222 mL in 1 BOTTLE, PUMP (36800-169-08)

NDC Information of ANTIBACTERIAL FOAMING

NDC Code 36800-169-08
Proprietary Name ANTIBACTERIAL FOAMING
Package Description 222 mL in 1 BOTTLE, PUMP (36800-169-08)
Product NDC 36800-169
Product Type Name HUMAN OTC DRUG
Non Proprietary Name TRICLOSAN
Dosage Form Name LIQUID
Route Name TOPICAL
Start Marketing Date 20111101
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name TOPCO ASSOCIATES LLC
Substance Name TRICLOSAN
Strength Number .46
Strength Unit mL/100mL
Pharmaceutical Classes

Complete Information of ANTIBACTERIAL FOAMING


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