nu-derm system normal-oily skin transformation trial is a Kit in the Human Prescription Drug category. It is labeled and distributed by Omp, Inc.. The primary component is .
| Product ID | 62032-515_8e028c28-495c-43d9-a48c-c718fb21530b |
| NDC | 62032-515 |
| Product Type | Human Prescription Drug |
| Proprietary Name | nu-derm system normal-oily skin transformation trial |
| Generic Name | Hydroquinone, Octinoxate, And Zinc Oxide |
| Dosage Form | Kit |
| Marketing Start Date | 2012-11-07 |
| Marketing Category | UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER |
| Labeler Name | OMP, INC. |
| Active Ingredient Strength | 0 |
| NDC Exclude Flag | N |
| Listing Certified Through | 2020-12-31 |
| Marketing Start Date | 2012-11-07 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | Unapproved drug other |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2012-11-07 |
| SPL SET ID: | c3957a49-4953-4e60-8213-6dc2ce5acff6 |
| Manufacturer | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 62032-533 | NU-DERM system NORMAL-oily SKIN TRANSFORMATION TRIAL | NU-DERM system NORMAL-oily SKIN TRANSFORMATION TRIAL |
| 62032-510 | CONDITION AND ENHANCE SYSTEM | HYDROQUINONE, OCTINOXATE, AND ZINC OXIDE |
| 62032-516 | nu-derm system normal-dry | Hydroquinone, Octinoxate, and Zinc Oxide |
| 62032-520 | NU-DERM SYSTEM NORMAL-DRY | Hydroquinone, Octinoxate, and Zinc Oxide |
| 62032-513 | NU-DERM SYSTEM NORMAL-OILY | Hydroquinone, Octinoxate, and Zinc Oxide |
| 62032-515 | nu-derm system normal-oily | Hydroquinone, Octinoxate, and Zinc Oxide |