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