OBAGI-C RX SYSTEM NORMAL-OILY 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 | 62032-517_ba2c32e0-568f-419b-8798-a75bc089cb2d |
| NDC | 62032-517 |
| Product Type | Human Prescription Drug |
| Proprietary Name | OBAGI-C RX SYSTEM NORMAL-OILY SKIN INTERVENTION |
| 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 | E |
| Listing Certified Through | 2018-12-31 |
| 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 |
| Inactivation Date | 2020-01-31 |
| SPL SET ID: | 80cc66d6-325c-4203-bb11-e655939d8b46 |
| Manufacturer | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 62032-534 | OBAGI-C RX system NORMAL-oily SKIN INTERVENTION | OBAGI-C RX system NORMAL-oily 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 |