Obagi Medical – Nu-Derm System – Normal to Dry – Skin Transformation Kit (OMP, Inc.)
Welcome to the PulseAid listing for the Obagi Medical – Nu-Derm System – Normal to Dry – Skin Transformation Kit drug offered from OMP, Inc.. This pharmaceutical is classified as a HUMAN OTC 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 OTC DRUG drug type category.
| LABELER NAME / MANUFACTURER: | OMP, Inc. |
| NON-PROPRIETARY NAME: | OCTINOXATE, ZINC OXIDE |
| SUBSTANCE NAME: | |
| TYPE: | HUMAN OTC DRUG |
| PHARMA CLASS: | |
| ROUTE: | |
| DOSAGE FORM: | KIT |
| MARKETING CATEGORY NAME: | UNAPPROVED DRUG OTHER |
| START MARKETING DATE: | 2015-12-10 |
| END MARKETING DATE: | 0000-00-00 |
Obagi Medical – Nu-Derm System – Normal to Dry – Skin Transformation Kit HUMAN OTC DRUG Details:
| Item Description | Obagi Medical – Nu-Derm System – Normal to Dry – Skin Transformation Kit from OMP, Inc. |
| LABELER NAME: | OMP, Inc. |
| DEA SCHEDULE: | |
| ACTIVE STRENGTH: | () |
| START MARKETING DATE: | 2015-12-10 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 62032-526_935a1c17-63d7-43ba-b02c-0736c0ca1277 |
| PRODUCT NDC: | 62032-526 |
| APPLICATION NUMBER: |