NU-DERM system NORMAL-DRY SKIN TRANSFORMATION TRIAL is a Kit in the Human Prescription Drug category. It is labeled and distributed by Obagi Cosmeceutical Llc. The primary component is .
| Product ID | 62032-532_bc3a5f08-df7e-46a7-8a28-33f0b10a042e | 
| NDC | 62032-532 | 
| Product Type | Human Prescription Drug | 
| Proprietary Name | NU-DERM system NORMAL-DRY SKIN TRANSFORMATION TRIAL | 
| Generic Name | Hydroquinone, Homosalate, Octisalate, And Zinc Oxide | 
| Dosage Form | Kit | 
| Marketing Start Date | 2019-12-02 | 
| Marketing Category | UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER | 
| Labeler Name | OBAGI COSMECEUTICAL LLC | 
| Active Ingredient Strength | 0 | 
| NDC Exclude Flag | N | 
| Listing Certified Through | 2022-12-31 | 
| Marketing Start Date | 2019-12-02 | 
| NDC Exclude Flag | N | 
| Sample Package? | N | 
| NDC | Brand Name | Generic Name | 
|---|---|---|
| 62032-522 | NU-DERM SYSTEM NORMAL-DRY SKIN TRANSFORMATION TRIAL | NU-DERM SYSTEM NORMAL-DRY SKIN TRANSFORMATION TRIAL | 
| 62032-516 | NU-DERM SYSTEM NORMAL-DRY SKIN TRANSFORMATION TRIAL | NU-DERM SYSTEM NORMAL-DRY SKIN TRANSFORMATION TRIAL | 
| 62032-532 | NU-DERM system NORMAL-DRY | Hydroquinone, Homosalate, Octisalate, and Zinc Oxide | 
| 62032-531 | NU-DERM System NORMAL-Oily | HYDROQUINONE, HOMOSALATE, OCTISALATE, and ZINC OXIDE | 
| 62032-533 | NU-DERM system NORMAL-oily | Hydroquinone, Homosalate, Octisalate, and Zinc Oxide | 
| 62032-535 | OBAGI-C RX System NORMAL-DRY | HYDROQUINONE, HOMOSALATE, OCTISALATE, AND ZINC OXIDE |