# FDA recall D-0257-2021

> **DLC Laboratories, Inc** · Class II · drug recall initiated 2021-01-06.

## 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.

## Distribution

Distributed Nationwide and to the following foreign countries: Canada, Cambodia, Germany, and United Kingdom.

## Key facts

- **Recall number:** D-0257-2021
- **Recalling firm:** DLC Laboratories, Inc
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2021-01-06
- **Report date:** 2021-02-24
- **Termination date:** 2022-09-23

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Paramount, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0257-2021

## Citation

> AI Analytics. FDA recall D-0257-2021. Retrieved 2026-08-19 from https://api.ai-analytics.org/recall/D-0257-2021. Source: US FDA. Licensed CC0.

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