June 21, 2001LotriminÆ AF Spray Liquid
TN (SafetyAlerts) - The Food and
Drug Administration (FDA) said today that Schering-Plough HealthCare Products has recalled
certain LotriminÆ AF Spray Liquid because it is misbranded; Lotrimin AF Liquid Spray was
incorrectly labeled as Lotrimin AF Deodorant Powder.
This is the first public notice of
this Class III
recall issued by FDA.
LotriminÆ AF Spray Liquid, 4 oz. (113 gram) Aerosol can, The product is an OTC,
topically applied antifungal aerosol. The active ingredient is 2% Miconazole Nitrate.
Recall # D-221-1.
Lot Number 1A05CC. 1A05CCC Exp 01 04.
CCL Custom Manufacturing, Inc. Cumberland, RI.
Schering-Plough HealthCare Products, Cleveland, TN., by letter dated May 22, 2001.
Firm-initiated recall ongoing.
96,500 units (individual cans).
Questions concerning this recall may be directed
to the FDA at 1-888-INFO-FDA.
Notice of this product warning was sent via email
to SafetyAlerts subscribers June 21,
2001. For more information regarding the SafetyAlerts free email alert service
please click here.