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SafetyAlerts
December 28, 1999

Consumer Health Care Group Recalls HemoridÆ Hemorrhoidal Suppositories

Parsippany, NJ (SafetyAlerts) - The Food and Drug Administration (FDA) today reported that Consumer Health Care Group is recalling HemoridÆ Hemorrhoidal Suppositories, made by G&W Laboratories, Inc. because of subpotency of phenylephrine (stability testing).

This ongoing Class III recall was initiated by the company by letter on or about October 29, 1998.  This is the first public notice issued by the FDA.

The HemoridÆ Hemorrhoidal Suppositories, (Zinc Oxide 11%/Phenylephrine Hydrochloride 0.25%), was sold Nationwide and in Puerto Rico, in boxes of 12. The recall affects all unexpired lots, over 1,227,948 units.  The firm estimates none remains on the market.

Questions concerning this recall may be directed to the FDA at 1-888-INFO-FDA.

 
Selected Recent Recalls


Health Professional:

Did you know?
During 2000 there were over
1050 products recalled in the United
States for safety reasons!

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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.