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KPP Ultra Thick Medicated Callus Remover - 61715-071-04 - (Salicylic Acid)

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Drug Information of KPP Ultra Thick Medicated Callus Remover

Product NDC: 61715-071
Proprietary Name: KPP Ultra Thick Medicated Callus Remover
Non Proprietary Name: Salicylic Acid
Active Ingredient(s): 40    1/1 & nbsp;   Salicylic Acid
Administration Route(s): TOPICAL
Dosage Form(s): PLASTER
Coding System: National Drug Codes(NDC)

Labeler Information of KPP Ultra Thick Medicated Callus Remover

Product NDC: 61715-071
Labeler Name: Cardinal Health
Product Type: HUMAN OTC DRUG
FDA Application Number: part358F
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 19951031

Package Information of KPP Ultra Thick Medicated Callus Remover

Package NDC: 61715-071-04
Package Description: 4 PLASTER in 1 PACKET (61715-071-04)

NDC Information of KPP Ultra Thick Medicated Callus Remover

NDC Code 61715-071-04
Proprietary Name KPP Ultra Thick Medicated Callus Remover
Package Description 4 PLASTER in 1 PACKET (61715-071-04)
Product NDC 61715-071
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Salicylic Acid
Dosage Form Name PLASTER
Route Name TOPICAL
Start Marketing Date 19951031
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Cardinal Health
Substance Name SALICYLIC ACID
Strength Number 40
Strength Unit 1/1
Pharmaceutical Classes

Complete Information of KPP Ultra Thick Medicated Callus Remover


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