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Wart Remover
Wart Remover - 28691-0838-1 - (Salicylic Acid)
Drug Information of Wart Remover
| Product NDC: | 28691-0838 |
| Proprietary Name: | Wart Remover |
| Non Proprietary Name: | Salicylic Acid |
| Active Ingredient(s): | 40 mL/1 & nbsp; Salicylic Acid |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | PLASTER |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Wart Remover
| Product NDC: | 28691-0838 |
| Labeler Name: | Pharmaplast SAE |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part358B |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100901 |
Package Information of Wart Remover
| Package NDC: | 28691-0838-1 |
| Package Description: | 20 PLASTER in 1 BOX (28691-0838-1) |
NDC Information of Wart Remover
| NDC Code | 28691-0838-1 |
| Proprietary Name | Wart Remover |
| Package Description | 20 PLASTER in 1 BOX (28691-0838-1) |
| Product NDC | 28691-0838 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Salicylic Acid |
| Dosage Form Name | PLASTER |
| Route Name | TOPICAL |
| Start Marketing Date | 20100901 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Pharmaplast SAE |
| Substance Name | SALICYLIC ACID |
| Strength Number | 40 |
| Strength Unit | mL/1 |
| Pharmaceutical Classes |
