Obagi Nu-Derm Clear — Class II drug recall D-0234-2015
Terminated recall by Obagi Medical Products, reported 2014-11-12, distributed nationwide. Labeling: Label Mix-Up; Containers of the Obagi Nu-Derm Clear pre-labeled bottles were inadvertently introduce
| Recall number | D-0234-2015 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Obagi Medical Products, Irvine, CA, United States |
| Recall initiated | 2014-10-17 |
| Classified | 2014-10-31 |
| Reported by FDA | 2014-11-12 |
| Terminated | 2015-04-29 |
| Distributed | Nationwide (US) |
| Countries outside the US | MX, SI |
| Quantity | 975 bottles |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 00362032101361 |
| NDC | 62032-0100-36, 62032-0101-36, 62032-0140-09, 62032-0912, 62032-0912-01 |
| Lot numbers | 13I1218 |
| Model numbers | 362032101361 |
| Expiration dates | 2016-09-30 |
Product
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
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0234-2015. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.