Mcneil Consumer Healthcare Recalls Four Product Lots of Benadryl® Allergy Ultratab[TM] Tablets, 100 Count, and One Product Lot of Extra Strength Tylenol® Rapid Release Gels, 50 Count

"U.S. Food & Drug Administration (FDA)" <fda@xxxxxxxxxxxxxxxxxxxxxxx> · Thu, 17 Jun 2010 10:12:22 -0500 (CDT)

Title: Mcneil Consumer Healthcare Recalls Four Product Lots of Benadryl® Allergy Ultratab[TM] Tablets, 100 Count, and One Product Lot of Extra Strength Tylenol® Rapid Release Gels, 50 Count

McNeil Consumer Healthcare Recalls Four Product Lots of Benadryl® Allergy Ultratab[TM] Tablets, 100 Count, and One Product Lot of Extra Strength Tylenol® Rapid Release Gels, 50 Count

Thu, 17 Jun 2010 09:50:00 -0500

Fort Washington, PA (June 15, 2010) – McNeil Consumer Healthcare, Division of McNEIL-PPC, Inc., is recalling five product lots as an addition to the list of products included in the company’s January 15th, 2010 product recall. The additional lots involved are four product lots of BENADRYL® ALLERGY ULTRATAB™ TABLETS, 100 count, sold in the U.S.; and one product lot of EXTRA STRENGTH TYLENOL® Rapid Release Gels, 50 count sold in the U.S., Trinidad and Tobago, Bermuda,
 and Puerto Rico.

Manage your FDA Subscriptions:

  Update your preferences or unsubscribe

  Questions about this service? support@xxxxxxxxxxxxxxx

  Other inquiries? webmail@xxxxxxxxxx

			GovDelivery, Inc. sending on behalf of U.S. Food & Drug Administration (FDA)
			· 10903 New Hampshire Ave

			· 10903 New Hampshire Ave MD 20993
			· 800-439-1420