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 Divis…

Recall date

January 6, 2021

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

D-0257-2021

FDA classification

Class II

Brand / firm

DLC Laboratories, Inc

Sold / distributed

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

Why it was recalled

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

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

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