NU-DERM SYSTEM NORMAL-DRY SKIN TRANSFORMATION is a Kit in the Human Prescription Drug category. It is labeled and distributed by Omp, Inc.. The primary component is .
| Product ID | 62032-520_1be2dfad-d98e-4b0d-9d07-4820deb8e2aa |
| NDC | 62032-520 |
| Product Type | Human Prescription Drug |
| Proprietary Name | NU-DERM SYSTEM NORMAL-DRY SKIN TRANSFORMATION |
| Generic Name | Hydroquinone, Octinoxate, And Zinc Oxide |
| Dosage Form | Kit |
| Marketing Start Date | 2013-04-15 |
| Marketing Category | UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER |
| Labeler Name | OMP, INC. |
| Active Ingredient Strength | 0 |
| NDC Exclude Flag | E |
| Listing Certified Through | 2018-12-31 |
| Marketing Start Date | 2013-04-15 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | Unapproved drug other |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2013-04-15 |
| Inactivation Date | 2020-01-31 |
| SPL SET ID: | 0d91be8e-1553-4ef7-b333-724c0e27651e |
| Manufacturer | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 62032-514 | NU-DERM SYSTEM NORMAL-DRY SKIN TRANSFORMATION | NU-DERM SYSTEM NORMAL-DRY SKIN TRANSFORMATION |
| 62032-529 | nu-derm system normal-dry skin transformation | nu-derm system normal-dry skin transformation |
| 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 |