Drug recall
Sulfur Ointment 10%, Pomada de Azufre, 2.6 OZ (73.7g) jar; Manufactured by/ Fabricado por: De La Cruz…
FDA recall event 87257 · Class II · DLC Laboratories, Inc
Key facts
| Event ID | 87257 |
|---|---|
| Recall numbers | D-0257-2021 |
| Recalling firm | DLC Laboratories, Inc |
| Product type | Drugs |
| Products | 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 |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary: Firm Initiated |
| Reason for recall | Labeling: Label Mix-Up. THe English label with Drug Facts panel for Camphor was incorrectly placed on product. |
| Initiation date | Jan 6, 2021 |
| Report date | Feb 24, 2021 |
| Termination date | Sep 23, 2022 |
| City | Paramount |
| State | CA |
| Country | United States |
| FEI number | 2020223 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: