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Wyeth Consumer Healthcare is voluntarily recalling the above two lots of .41 fl. oz. Anbesol Maximum
Strength Liquid listed above. Some of the bottles of product may be subpotent; however, the subpotency does
not compromise the safety of these lots. In addition to the open stock, a portion of Anbesol Maximum
Strength Liquid, Lot B65043 was sold in the display lots listed above. This recall is extended to the retail
shelf level.
These products were shipped during the period of March 2006 through January 2007.
Disposition:
Please examine your inventory for the affected items completely and stop dispensing immediately. If you
have any of the affected lot numbers, using your Telxon or Econolink, please transmit a request for return
authorization as unsaleable, manufacturer recall, and return within 30 days to your McKesson servicing
distribution center for credit.
NOTE: For All Recalled Product Not In Original Containers: Please note NDC#, Lot#, expiration date
on the outside of the container for all product being returned that is not in the original manufacturer
container. Any product received without this information will be returned to the customer without being
processed.
The Food and Drug Administration has full knowledge of this voluntary recall.
If you have any questions, please call the Product Quality Department at 1-800-762-4675.
(Information contained in this document was provided by Wyeth Consumer HeaIthcare.)
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