Reported Feb 24, 2021 · Terminated

Sulfur Ointment 10%, Pomada de Azufre, 2.6 OZ (73.7g) jar; Manufactured by/ Fabricado por: De La Cruz Products, A…

DLC Laboratories, Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: DLC Laboratories, Inc · 7008 Marcelle St · Paramount, CA · 90723-4839

Is this the product you have?

    • Sulfur Ointment 10%
    • Pomada de Azufre
    • 2.6 OZ (73.7g) jar
  • Manufactured by/ Fabricado porDe La Cruz Products, A Division of DLC Laboratories, Inc. Paramount, CA 9023 USA; UPC 024286150426
Lot codes and dates
    • Lot # 5084
    • Exp 05/23
    • 5130
    • Exp 07/23
    • 5132
    • Exp 07/23
    • 5160
    • Exp 08/23
Amount recalled
86,297 jars

Where it was sold

  • Nationwide

Why it was recalled

Labeling: Label Mix-Up. THe English label with Drug Facts panel for Camphor was incorrectly placed on product.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

Free recall alerts

Get alerted about new DLC Laboratories, Inc. recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA drug enforcement) notice

Notice updated Sep 23, 2022 · Data as of Sep 19, 8:09 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.