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SafetyAlerts
July 23, 2003

Recall Update: Denison Pharmaceuticals Decolorized IODINE TINCTURE Recall is Complete

(SafetyAlerts) - The Food and Drug Administration (FDA) released the following information.

PRODUCT
Decolorized IODINE TINCTURE, (Alcohol 41-45%, Iodine 3%, Potassium Iodide 1.5%), 1 FLUID OUNCE bottle, POISON. Recall # D-281-3.

CODE
All lot codes.

RECALLING FIRM/MANUFACTURER
Denison Pharmaceuticals, Inc., Pawtucket, RI, by telephone on May 14, 2003. Firm initiated recall is complete.

REASON
Mislabeled; product contains undeclared ammonium hydroxide.

VOLUME OF PRODUCT IN COMMERCE
794 bottles.

DISTRIBUTION
Nationwide
.

 
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The information contained herein has been obtained from sources that the Company believes to be reliable, however, the Company has not independently verified or confirmed the information and the recipient acknowledges that no representations or warranties are being made in connection with the use of the information.