US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jan 6, 2021 (6 years ago)

Sulfur Ointment 10%, Pomada de Azufre, 2.6 OZ (73.7g) jar; Manufactured by/ Fabricado…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

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

What was recalled

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

Recalling firm
DLC Laboratories, Inc
Origin
CA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0257-2021

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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