NDC 99207-225 is a in the category. It is labeled and distributed by Medicis Pharmaceutical Corp.
| Product ID | 99207-225_d6cba3eb-ba05-4294-a2fe-42eb1150f3f1 |
| NDC | 99207-225 |
| Proprietary Name | NDC 99207-225 |
| Marketing Start Date | 2011-07-21 |
| Marketing Category | / |
| Labeler Name | Medicis Pharmaceutical Corp |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | UNAPPROVED DRUG OTHER |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2010-01-14 |
| Marketing End Date | 2011-03-04 |
| Marketing Category | UNAPPROVED DRUG OTHER |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2009-03-15 |
| Marketing End Date | 2011-03-04 |
| Marketing Category | UNAPPROVED DRUG OTHER |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2010-01-14 |
| Marketing End Date | 2011-03-04 |
| Ingredient | Strength |
|---|---|
| BENZOYL PEROXIDE | 60 mg/g |