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: |