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Umecta Mousse
Umecta Mousse - 68712-020-01 - (Urea Foam)
Drug Information of Umecta Mousse
| Product NDC: | 68712-020 |
| Proprietary Name: | Umecta Mousse |
| Non Proprietary Name: | Urea Foam |
| Active Ingredient(s): | 400 mg/g & nbsp; Urea Foam |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | AEROSOL, FOAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Umecta Mousse
| Product NDC: | 68712-020 |
| Labeler Name: | Innocutis Holdings LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20070901 |
Package Information of Umecta Mousse
| Package NDC: | 68712-020-01 |
| Package Description: | 113.4 g in 1 CAN (68712-020-01) |
NDC Information of Umecta Mousse
| NDC Code | 68712-020-01 |
| Proprietary Name | Umecta Mousse |
| Package Description | 113.4 g in 1 CAN (68712-020-01) |
| Product NDC | 68712-020 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Urea Foam |
| Dosage Form Name | AEROSOL, FOAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20070901 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Innocutis Holdings LLC |
| Substance Name | UREA |
| Strength Number | 400 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
