FDAFDA · Food and drugs·Recall number D-0234-2015
Obagi Nu-Derm Clear, AM PM 3, Skin Bleaching and Corrector Cream, Hydroquinone USP, 4%, Rx Only, Net Wt. 2 OZ. (57 g) bottle, Dist by OMP Inc, Long Beach CA 90802, Made in USA, NDC 62032-101-36
Published November 12, 2014 · Recall initiated: October 17, 2014
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
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.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- OBAGI NU-DERM SYSTEM NORMAL-OILY SKIN TRANSFORMATION
- Manufacturer
- Obagi Medical Products
- Distributor
- Nationwide and Mexico and Slovenia
- UPC
- 362032101361
- Lot
- Lot #: 13I1218, Product/Part #: 362032101361, Exp 09/30/2016
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
Sell products like this?
Recalert watches your whole catalog for recalls like this one, automatically.