July 23, 2003
Recall Update: Denison Pharmaceuticals
Decolorized IODINE TINCTURE Recall is Complete
The Food and Drug Administration (FDA) released the following information.
Decolorized IODINE TINCTURE, (Alcohol 41-45%, Iodine 3%, Potassium Iodide
1.5%), 1 FLUID OUNCE bottle, POISON. Recall # D-281-3.
All lot codes.
Denison Pharmaceuticals, Inc., Pawtucket, RI, by telephone on May 14, 2003.
Firm initiated recall is complete.
Mislabeled; product contains undeclared ammonium hydroxide.
VOLUME OF PRODUCT IN COMMERCE