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ANTIBACTERIAL FOAMING - 55316-163-32 - (TRICLOSAN)

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Drug Information of ANTIBACTERIAL FOAMING

Product NDC: 55316-163
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: 55316-163
Labeler Name: DZA BRANDS LLC
Product Type: HUMAN OTC DRUG
FDA Application Number: part333E
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20110322

Package Information of ANTIBACTERIAL FOAMING

Package NDC: 55316-163-32
Package Description: 946 mL in 1 BOTTLE (55316-163-32)

NDC Information of ANTIBACTERIAL FOAMING

NDC Code 55316-163-32
Proprietary Name ANTIBACTERIAL FOAMING
Package Description 946 mL in 1 BOTTLE (55316-163-32)
Product NDC 55316-163
Product Type Name HUMAN OTC DRUG
Non Proprietary Name TRICLOSAN
Dosage Form Name LIQUID
Route Name TOPICAL
Start Marketing Date 20110322
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name DZA BRANDS LLC
Substance Name TRICLOSAN
Strength Number .46
Strength Unit mL/100mL
Pharmaceutical Classes

Complete Information of ANTIBACTERIAL FOAMING


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