FDA Drug recall D-0257-2021
Sulfur Ointment 10%, Pomada de Azufre, 2.6 OZ (73.7g) jar
- FDA Drug
- Class II
- terminated
- Published 2021-02-24
On 2021-02-24 the FDA classified a Class II recall of Sulfur Ointment 10%, Pomada de Azufre, 2.6 OZ (73.7g) jar by Dlc Laboratories, citing labeling: Label Mix-Up. THe English label with Drug Facts panel for Camphor was incorrectly placed on product.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0257-2021 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2021-01-06 |
| Published | 2021-02-24 |
| Last updated | 2026-09-13 11:52 UTC |
| Company | Dlc Laboratories |
| Distribution | US |
Product
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
Labeling: Label Mix-Up. THe English label with Drug Facts panel for Camphor was incorrectly placed on product.
Identifiers
| upc | 024286150426 |
|---|---|
| code_info | Lot # 5084, Exp 05/23; 5130, Exp 07/23; 5132, Exp 07/23; 5160, Exp 08/23. |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0257-2021%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.