NU-DERM TRAVEL SET NORMAL/DRYSKIN TRANSFORMATION SYSTEM (OMP, INC.)
Welcome to the PulseAid listing for the NU-DERM TRAVEL SET NORMAL/DRY drug offered from OMP, INC.. This pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
| LABELER NAME / MANUFACTURER: | OMP, INC. |
| NON-PROPRIETARY NAME: | HYDROQUINONE, OCTINOXATE AND ZINC OXIDE |
| SUBSTANCE NAME: | |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | |
| ROUTE: | |
| DOSAGE FORM: | KIT |
| MARKETING CATEGORY NAME: | UNAPPROVED DRUG OTHER |
| START MARKETING DATE: | 2004-12-02 |
| END MARKETING DATE: | 0000-00-00 |
NU-DERM TRAVEL SET NORMAL/DRY SKIN TRANSFORMATION SYSTEM HUMAN PRESCRIPTION DRUG Details:
| Item Description | NU-DERM TRAVEL SET NORMAL/DRY SKIN TRANSFORMATION SYSTEM from OMP, INC. |
| LABELER NAME: | OMP, INC. |
| DEA SCHEDULE: | |
| ACTIVE STRENGTH: | () |
| START MARKETING DATE: | 2004-12-02 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 62032-500_2f665c58-4e09-4531-903f-ad747b483d6b |
| PRODUCT NDC: | 62032-500 |
| APPLICATION NUMBER: |