Product NDC: | 42808-200 |
Proprietary Name: | Urea |
Non Proprietary Name: | Urea |
Active Ingredient(s): | 500 mg/g & nbsp; Urea |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 42808-200 |
Labeler Name: | Exact-Rx, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20110801 |
Package NDC: | 42808-200-05 |
Package Description: | 1 TUBE in 1 CARTON (42808-200-05) > 142 g in 1 TUBE |
NDC Code | 42808-200-05 |
Proprietary Name | Urea |
Package Description | 1 TUBE in 1 CARTON (42808-200-05) > 142 g in 1 TUBE |
Product NDC | 42808-200 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Urea |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20110801 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Exact-Rx, Inc. |
Substance Name | UREA |
Strength Number | 500 |
Strength Unit | mg/g |
Pharmaceutical Classes |