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Vanilla Cupcake Anti Bacterial Foaming Hand - 59021-005-01 - (TRICLOSAN)

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Drug Information of Vanilla Cupcake Anti Bacterial Foaming Hand

Product NDC: 59021-005
Proprietary Name: Vanilla Cupcake Anti Bacterial Foaming Hand
Non Proprietary Name: TRICLOSAN
Active Ingredient(s): .3    g/100mL & nbsp;   TRICLOSAN
Administration Route(s): TOPICAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Vanilla Cupcake Anti Bacterial Foaming Hand

Product NDC: 59021-005
Labeler Name: Five Below
Product Type: HUMAN OTC DRUG
FDA Application Number: part333E
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20130413

Package Information of Vanilla Cupcake Anti Bacterial Foaming Hand

Package NDC: 59021-005-01
Package Description: 225 mL in 1 BOTTLE (59021-005-01)

NDC Information of Vanilla Cupcake Anti Bacterial Foaming Hand

NDC Code 59021-005-01
Proprietary Name Vanilla Cupcake Anti Bacterial Foaming Hand
Package Description 225 mL in 1 BOTTLE (59021-005-01)
Product NDC 59021-005
Product Type Name HUMAN OTC DRUG
Non Proprietary Name TRICLOSAN
Dosage Form Name LIQUID
Route Name TOPICAL
Start Marketing Date 20130413
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Five Below
Substance Name TRICLOSAN
Strength Number .3
Strength Unit g/100mL
Pharmaceutical Classes

Complete Information of Vanilla Cupcake Anti Bacterial Foaming Hand


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