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Plantar Wart Removers
Plantar Wart Removers - 56104-018-24 - (Plantar Wart Removers)
Drug Information of Plantar Wart Removers
| Product NDC: | 56104-018 |
| Proprietary Name: | Plantar Wart Removers |
| Non Proprietary Name: | Plantar Wart Removers |
| Active Ingredient(s): | 40 mg/100mg & nbsp; Plantar Wart Removers |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | PATCH |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Plantar Wart Removers
| Product NDC: | 56104-018 |
| Labeler Name: | Premier Brands of America Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part358B |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130101 |
Package Information of Plantar Wart Removers
| Package NDC: | 56104-018-24 |
| Package Description: | 24 mg in 1 BOX (56104-018-24) |
NDC Information of Plantar Wart Removers
| NDC Code | 56104-018-24 |
| Proprietary Name | Plantar Wart Removers |
| Package Description | 24 mg in 1 BOX (56104-018-24) |
| Product NDC | 56104-018 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Plantar Wart Removers |
| Dosage Form Name | PATCH |
| Route Name | TOPICAL |
| Start Marketing Date | 20130101 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Premier Brands of America Inc. |
| Substance Name | SALICYLIC ACID |
| Strength Number | 40 |
| Strength Unit | mg/100mg |
| Pharmaceutical Classes |
