NDC 62032-912
Obagi Nu-Derm System Normal-Oily Skin Transformation 5 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 |
| Swiss-American CDMO, LLC | Carrollton, TX, United States | Makes it | Problems found, fixed voluntarilyMar 31, 2022 · 6 inspections |
| Bay Cities Container Corporation | Santa Fe Springs, CA, United States | Packages it and labels it | Not inspected on record |
Recalls
- Oct 17, 2014 · Class II · Obagi Medical Products
Labeling: Label Mix-Up; Containers of the Obagi Nu-Derm Clear pre-labeled bottles were inadvertently introduced into the Obagi Exfoderm Forte packaging line. Therefore customers which ordered Clear RX actually had contents of Exfoderm forte.
Lots: Lot #: 13I1218, Product/Part #: 362032101361, Exp 09/30/2016
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Hydroquinone, Homosalate, Octisalate and Zinc Oxide: every company that makes it
- Form
- kit
- Strength
- 5 ingredients
- Approval
- UNAPPROVED DRUG OTHER
- On the market since
- Jun 25, 2021
- Package NDCs
62032-100-3662032-101-3662032-140-0962032-912-01- Official label
- DailyMed (National Library of Medicine), updated Oct 23, 2025
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