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Wart Remover Gel
Wart Remover Gel - 56104-237-07 - (Wart Remover Gel)
Drug Information of Wart Remover Gel
| Product NDC: | 56104-237 |
| Proprietary Name: | Wart Remover Gel |
| Non Proprietary Name: | Wart Remover Gel |
| Active Ingredient(s): | .17 g/g & nbsp; Wart Remover Gel |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Wart Remover Gel
| Product NDC: | 56104-237 |
| 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 Wart Remover Gel
| Package NDC: | 56104-237-07 |
| Package Description: | 7 g in 1 TUBE (56104-237-07) |
NDC Information of Wart Remover Gel
| NDC Code | 56104-237-07 |
| Proprietary Name | Wart Remover Gel |
| Package Description | 7 g in 1 TUBE (56104-237-07) |
| Product NDC | 56104-237 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Wart Remover Gel |
| Dosage Form Name | GEL |
| 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 | .17 |
| Strength Unit | g/g |
| Pharmaceutical Classes |
