FDAFDA · Food and drugs·Recall number D-0257-2021
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
Published February 24, 2021 · Recall initiated: January 6, 2021
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Labeling: Label Mix-Up. THe English label with Drug Facts panel for Camphor was incorrectly placed on product.
What to do
Voluntary: Firm initiated · E-Mail
Recall details
- Manufacturer
- DLC Laboratories, Inc
- Distributor
- Distributed Nationwide and to the following foreign countries: Canada, Cambodia, Germany, and United Kingdom.
- Lot
- Lot # 5084, Exp 05/23; 5130, Exp 07/23; 5132, Exp 07/23; 5160, Exp 08/23.
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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