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 |