NDC 62032-522
nu-derm system normal-dry skin 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 |
| 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
- Apr 15, 2013
- Package NDCs
62032-522-60- Official label
- DailyMed (National Library of Medicine), updated Nov 14, 2019
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