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Cornex
Cornex - 56104-009-09 - (Corn and Callus Liquid Remover)
Drug Information of Cornex
| Product NDC: | 56104-009 |
| Proprietary Name: | Cornex |
| Non Proprietary Name: | Corn and Callus Liquid Remover |
| Active Ingredient(s): | .17 g/g & nbsp; Corn and Callus Liquid Remover |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cornex
| Product NDC: | 56104-009 |
| Labeler Name: | Premier Brands of America Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part358F |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130101 |
Package Information of Cornex
| Package NDC: | 56104-009-09 |
| Package Description: | 9 g in 1 BOTTLE, WITH APPLICATOR (56104-009-09) |
NDC Information of Cornex
| NDC Code | 56104-009-09 |
| Proprietary Name | Cornex |
| Package Description | 9 g in 1 BOTTLE, WITH APPLICATOR (56104-009-09) |
| Product NDC | 56104-009 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Corn and Callus Liquid Remover |
| Dosage Form Name | LIQUID |
| 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 |
