DLC Laboratories Sulfur Ointment 10%, Pomada de Azufre, 2.6 OZ (73.7g) jar recall — FDA D-0257-2021
Labeling: Label Mix-Up. THe English label with Drug Facts panel for Camphor was incorrectly placed on product.
Overview of recall records associated with DLC Laboratories, Inc., including dates, categories and classifications where available.
Classification mix: Class II: 2.
Labeling: Label Mix-Up. THe English label with Drug Facts panel for Camphor was incorrectly placed on product.
Microbial Contamination of Non-Sterile Products.
This page summarizes recall records in which the official source identifies DLC Laboratories, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.