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

Recalled February 24, 2021 · FDA recall D-0257-2021 · DLC Laboratories

Hazard

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

Units

86,297 jars

Sold at

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

Description

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

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

Manufacturer(s)

DLC Laboratories, Inc

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →