D-0257-2021 Class II Terminated
FDA drug recall D-0257-2021 was initiated by DLC Laboratories, Inc on January 6, 2021 and is designated Class II. Reason for recall: Labeling: Label Mix-Up. THe English label with Drug Facts panel for Camphor was incorrectly placed on product. The recall status is terminated (terminated September 23, 2022). Affected quantity: 86,297 jars.
Recall Details
- Product Type
- Drugs
- Report Date
- February 24, 2021
- Initiation Date
- January 6, 2021
- Termination Date
- September 23, 2022
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 86,297 jars
Product Description
Sulfur Ointment 10%, Pomada de Azufre, 2.6 OZ (73.7g) jar; Manufactured by/ Fabricado por: De La Cruz Products, A Division of DLC Laboratories, Inc. Paramount, CA 9023 USA; UPC 024286150426
Reason for Recall
Labeling: Label Mix-Up. THe English label with Drug Facts panel for Camphor was incorrectly placed on product.
Distribution Pattern
Distributed Nationwide and to the following foreign countries: Canada, Cambodia, Germany, and United Kingdom.
Code Information
Lot # 5084, Exp 05/23; 5130, Exp 07/23; 5132, Exp 07/23; 5160, Exp 08/23.