Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Obagi Nu-Derm Clear Recalled by Obagi Medical Products Due to Labeling: Label Mix-Up; Containers of the Obagi Nu-Derm...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Obagi Medical Products directly.
Affected Products
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
Quantity: 975 bottles
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Obagi Medical Products
Obagi Medical Products has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report