NDC 62032-516
nu-derm system normal-dryskin transformation trial 4 ingredients kit
On the label: Omp, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| G.s. Cosmeceutical Usa, Inc. | Livermore, CA, United States | Makes it | Problems found, fixed voluntarilyAug 14, 2019 · 6 inspections, 1 with FDA action |
| Milbar Laboratories, Inc. | East Haven, CT, United States | Makes it | Problems found, fixed voluntarilyNov 7, 2024 · 7 inspections, 3 with FDA action |
| PureTek Corporation | San Fernando, CA, United States | Makes it, packages it and labels it | Problems found, fixed voluntarilyMar 7, 2025 · 10 inspections |
| Bay Cities Container Corporation | Pico Rivera, CA, United States | Repackages it and relabels it | Not inspected on record |
Product details
- Generic drug
- Hydroquinone and Octinoxate and Zinc Oxide: every company that makes it
- Form
- kit
- Strength
- 4 ingredients
- Approval
- Unapproved drug other
- On the market since
- Nov 7, 2012
- Package NDCs
62032-516-60- Official label
- DailyMed (National Library of Medicine), updated Dec 4, 2019
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?