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FOAMING ANTIBACTERIAL - 63148-173-08 - (TRICLOSAN)

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Drug Information of FOAMING ANTIBACTERIAL

Product NDC: 63148-173
Proprietary Name: FOAMING ANTIBACTERIAL
Non Proprietary Name: TRICLOSAN
Active Ingredient(s): .6    mL/100mL & nbsp;   TRICLOSAN
Administration Route(s): TOPICAL
Dosage Form(s): SOAP
Coding System: National Drug Codes(NDC)

Labeler Information of FOAMING ANTIBACTERIAL

Product NDC: 63148-173
Labeler Name: APOLLO HEALTH AND BEAUTY CARE
Product Type: HUMAN OTC DRUG
FDA Application Number: part333
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20100720

Package Information of FOAMING ANTIBACTERIAL

Package NDC: 63148-173-08
Package Description: 221 mL in 1 BOTTLE, PUMP (63148-173-08)

NDC Information of FOAMING ANTIBACTERIAL

NDC Code 63148-173-08
Proprietary Name FOAMING ANTIBACTERIAL
Package Description 221 mL in 1 BOTTLE, PUMP (63148-173-08)
Product NDC 63148-173
Product Type Name HUMAN OTC DRUG
Non Proprietary Name TRICLOSAN
Dosage Form Name SOAP
Route Name TOPICAL
Start Marketing Date 20100720
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name APOLLO HEALTH AND BEAUTY CARE
Substance Name TRICLOSAN
Strength Number .6
Strength Unit mL/100mL
Pharmaceutical Classes

Complete Information of FOAMING ANTIBACTERIAL


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