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 |