| Product NDC: | 11673-009 |
| Proprietary Name: | Liquid corn and Callus Remover |
| Non Proprietary Name: | Liquid corn and Callus Remover |
| Active Ingredient(s): | .17 g/g & nbsp; Liquid corn and Callus Remover |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 11673-009 |
| Labeler Name: | Target Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part358F |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130430 |
| Package NDC: | 11673-009-01 |
| Package Description: | 15 g in 1 BOTTLE, WITH APPLICATOR (11673-009-01) |
| NDC Code | 11673-009-01 |
| Proprietary Name | Liquid corn and Callus Remover |
| Package Description | 15 g in 1 BOTTLE, WITH APPLICATOR (11673-009-01) |
| Product NDC | 11673-009 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Liquid corn and Callus Remover |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20130430 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Target Corporation |
| Substance Name | SALICYLIC ACID |
| Strength Number | .17 |
| Strength Unit | g/g |
| Pharmaceutical Classes |