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Ulta Nectarine Spice Anti-Bacterial Gentle Foaming - 62296-0027-1 - (Triclosan)

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Drug Information of Ulta Nectarine Spice Anti-Bacterial Gentle Foaming

Product NDC: 62296-0027
Proprietary Name: Ulta Nectarine Spice Anti-Bacterial Gentle Foaming
Non Proprietary Name: Triclosan
Active Ingredient(s): .3    g/100g & nbsp;   Triclosan
Administration Route(s): TOPICAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Ulta Nectarine Spice Anti-Bacterial Gentle Foaming

Product NDC: 62296-0027
Labeler Name: Ulta
Product Type: HUMAN OTC DRUG
FDA Application Number: part333E
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20120601

Package Information of Ulta Nectarine Spice Anti-Bacterial Gentle Foaming

Package NDC: 62296-0027-1
Package Description: 242 g in 1 BOTTLE, PLASTIC (62296-0027-1)

NDC Information of Ulta Nectarine Spice Anti-Bacterial Gentle Foaming

NDC Code 62296-0027-1
Proprietary Name Ulta Nectarine Spice Anti-Bacterial Gentle Foaming
Package Description 242 g in 1 BOTTLE, PLASTIC (62296-0027-1)
Product NDC 62296-0027
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Triclosan
Dosage Form Name LIQUID
Route Name TOPICAL
Start Marketing Date 20120601
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Ulta
Substance Name TRICLOSAN
Strength Number .3
Strength Unit g/100g
Pharmaceutical Classes

Complete Information of Ulta Nectarine Spice Anti-Bacterial Gentle Foaming


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