| Product NDC: | 0168-0493 |
| Proprietary Name: | Urea |
| Non Proprietary Name: | urea |
| Active Ingredient(s): | 500 mg/g & nbsp; urea |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0168-0493 |
| Labeler Name: | E. FOUGERA & CO., A division of Nycomed US Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED OTHER |
| Start Marketing Date: | 20090915 |
| Package NDC: | 0168-0493-84 |
| Package Description: | 284 g in 1 TUBE (0168-0493-84) |
| NDC Code | 0168-0493-84 |
| Proprietary Name | Urea |
| Package Description | 284 g in 1 TUBE (0168-0493-84) |
| Product NDC | 0168-0493 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | urea |
| Dosage Form Name | SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20090915 |
| Marketing Category Name | UNAPPROVED OTHER |
| Labeler Name | E. FOUGERA & CO., A division of Nycomed US Inc. |
| Substance Name | UREA |
| Strength Number | 500 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |