Sulfur Ointment 10% — Class II drug recall D-0257-2021
Terminated recall by DLC Laboratories, Inc, reported 2021-02-24, distributed nationwide. Labeling: Label Mix-Up. THe English label with Drug Facts panel for Camphor was incorrectly placed on product.
| Recall number | D-0257-2021 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | DLC Laboratories, Inc, Paramount, CA, United States |
| Recall initiated | 2021-01-06 |
| Classified | 2021-02-12 |
| Reported by FDA | 2021-02-24 |
| Terminated | 2022-09-23 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA, DE, GB |
| Quantity | 86,297 jars |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 00024286150426 |
| Lot numbers | 05/23, 07/23, 08/23, 5084, 5130, 5132, 5160 |
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 for recall
Labeling: Label Mix-Up. THe English label with Drug Facts panel for Camphor was incorrectly placed on product.
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-0257-2021. 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.