NDC 62032-500
nu-derm travel set normal/dry skin transformation system 4 ingredients kit
On the label: Omp, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| PureTek Corporation | San Fernando, CA, United States | Makes it, packages it and labels it | Problems found, fixed voluntarilyMar 7, 2025 · 10 inspections |
| Swiss-American CDMO, LLC | Carrollton, TX, United States | Makes it | Problems found, fixed voluntarilyMar 31, 2022 · 6 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
- Dec 2, 2004
- Package NDCs
62032-500-60- Official label
- DailyMed (National Library of Medicine), updated Dec 4, 2019
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