NDC 62032-518
Obagi-C Rx System Normal-Dry Skin Intervention 4 ingredients kit
On the label: Omp, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Harmony Labs, Inc. | Location not on file | Makes it, tests it, packages it and labels it | Not inspected on record |
| 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
62032-105-3662032-106-1062032-121-9062032-518-04- Official label
- DailyMed (National Library of Medicine), updated Jan 2, 2013
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