| Product NDC: | 23710-035 |
| Proprietary Name: | Hydro 35 |
| Non Proprietary Name: | Urea in a water and lipid based foam containing lactic acid |
| Active Ingredient(s): | 35 g/100g & nbsp; Urea in a water and lipid based foam containing lactic acid |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | AEROSOL, FOAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 23710-035 |
| Labeler Name: | Quinnova Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED OTHER |
| Start Marketing Date: | 20090620 |
| Package NDC: | 23710-035-20 |
| Package Description: | 22 g in 1 CANISTER (23710-035-20) |
| NDC Code | 23710-035-20 |
| Proprietary Name | Hydro 35 |
| Package Description | 22 g in 1 CANISTER (23710-035-20) |
| Product NDC | 23710-035 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Urea in a water and lipid based foam containing lactic acid |
| Dosage Form Name | AEROSOL, FOAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20090620 |
| Marketing Category Name | UNAPPROVED OTHER |
| Labeler Name | Quinnova Pharmaceuticals, Inc. |
| Substance Name | UREA |
| Strength Number | 35 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |