Obagi Nu-Derm FX System – Normal to Dry (OMP, Inc.)
Welcome to the PulseAid listing for the Obagi Nu-Derm FX System – Normal to Dry 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: | OTC MONOGRAPH FINAL |
| START MARKETING DATE: | 2015-11-04 |
| END MARKETING DATE: | 0000-00-00 |
Obagi Nu-Derm FX System – Normal to Dry HUMAN OTC DRUG Details:
| Item Description | Obagi Nu-Derm FX System – Normal to Dry from OMP, Inc. |
| LABELER NAME: | OMP, Inc. |
| DEA SCHEDULE: | |
| ACTIVE STRENGTH: | () |
| START MARKETING DATE: | 2015-11-04 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 62032-527_50dcfca5-cb2d-452d-a5e9-050d6561b567 |
| PRODUCT NDC: | 62032-527 |
| APPLICATION NUMBER: | part352 |