| Product NDC: | 42192-115 |
| Proprietary Name: | UREA HYDRATING TOPICAL |
| Non Proprietary Name: | UREA |
| Active Ingredient(s): | 35 g/100g & nbsp; UREA |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | AEROSOL, FOAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 42192-115 |
| Labeler Name: | Acella Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20101109 |
| Package NDC: | 42192-115-15 |
| Package Description: | 150 g in 1 CANISTER (42192-115-15) |
| NDC Code | 42192-115-15 |
| Proprietary Name | UREA HYDRATING TOPICAL |
| Package Description | 150 g in 1 CANISTER (42192-115-15) |
| Product NDC | 42192-115 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | UREA |
| Dosage Form Name | AEROSOL, FOAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20101109 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Acella Pharmaceuticals |
| Substance Name | UREA |
| Strength Number | 35 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |