OBAGI-C RX SYSTEM NORMAL-DRY SKIN INTERVENTION is a Kit in the Human Prescription Drug category. It is labeled and distributed by Omp, Inc.. The primary component is .
Product ID | 62032-524_392f9428-6f3f-44ba-8719-fdf26aca7800 |
NDC | 62032-524 |
Product Type | Human Prescription Drug |
Proprietary Name | OBAGI-C RX SYSTEM NORMAL-DRY SKIN INTERVENTION |
Generic Name | Hydroquinone, Octinoxate And Zinc Oxide |
Dosage Form | Kit |
Marketing Start Date | 2013-04-02 |
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 | 2013-04-02 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | Unapproved drug other |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2013-04-02 |
Inactivation Date | 2020-01-31 |
SPL SET ID: | d3b35a0e-cce3-4601-b18f-3e615e3bcd25 |
Manufacturer | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
62032-535 | OBAGI-C RX System NORMAL-DRY SKIN INTERVENTION | OBAGI-C RX System NORMAL-DRY SKIN INTERVENTION |
62032-508 | CONDITION AND ENHANCE SYSTEM | HYDROQUINONE, OCTINOXATE AND ZINC OXIDE |
62032-509 | CONDITION AND ENHANCE SYSTEM | HYDROQUINONE, OCTINOXATE AND ZINC OXIDE |
62032-500 | NU-DERM TRAVEL SET NORMAL/DRY | HYDROQUINONE, OCTINOXATE AND ZINC OXIDE |
62032-518 | OBAGI-C RX SYSTEM NORMAL-DRY | HYDROQUINONE, OCTINOXATE AND ZINC OXIDE |
62032-524 | OBAGI-C RX SYSTEM NORMAL-DRY | HYDROQUINONE, OCTINOXATE AND ZINC OXIDE |
62032-517 | OBAGI-C RX SYSTEM NORMAL-OILY | HYDROQUINONE, OCTINOXATE AND ZINC OXIDE |
62032-523 | OBAGI-C RX SYSTEM NORMAL-OILY | HYDROQUINONE, OCTINOXATE AND ZINC OXIDE |