NDC 62032-101
NU-DERM CLEARSkin Bleaching and Corrector 40 mg per 1 g cream
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 |
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: every company that makes it
- Form
- cream, topical
- Strength
- 40 mg per 1 g
- Approval
- UNAPPROVED DRUG OTHER
- On the market since
- Jan 1, 1988
- Package NDCs
62032-101-36- Official label
- DailyMed (National Library of Medicine), updated Jan 1, 2025
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