PlainRecalls
FDA Drug Low Class III Terminated

Lamisil AT Cream (terbinafine hydrochloride 1% antifungal), 12 gm ( .42 oz) Tubes and 30 gm (1 oz) Tubes packaged in one box, Novartis Consumer Health, Inc., Parsitan, NJ. UPC code: 300676249438. (Club Pack), NDC 0067-6295-43

Reported: June 12, 2013 Initiated: February 19, 2013 #D-576-2013

Product Description

Lamisil AT Cream (terbinafine hydrochloride 1% antifungal), 12 gm ( .42 oz) Tubes and 30 gm (1 oz) Tubes packaged in one box, Novartis Consumer Health, Inc., Parsitan, NJ. UPC code: 300676249438. (Club Pack), NDC 0067-6295-43

Reason for Recall

Labeling: Incorrect or Missing Lot and/or Expiration date; The Lot and/or Expiration date on the tube may not be legible in this lot.

Details

Recalling Firm
Novartis Consumer Health
Units Affected
41,400 Boxes
Distribution
Nationwide and Puerto Rico, and Panama. Military distribution made.
Location
Lincoln, NE

Frequently Asked Questions

What product was recalled?
Lamisil AT Cream (terbinafine hydrochloride 1% antifungal), 12 gm ( .42 oz) Tubes and 30 gm (1 oz) Tubes packaged in one box, Novartis Consumer Health, Inc., Parsitan, NJ. UPC code: 300676249438. (Club Pack), NDC 0067-6295-43. Recalled by Novartis Consumer Health. Units affected: 41,400 Boxes.
Why was this product recalled?
Labeling: Incorrect or Missing Lot and/or Expiration date; The Lot and/or Expiration date on the tube may not be legible in this lot.
Which agency issued this recall?
This recall was issued by the FDA Drug on June 12, 2013. Severity: Low. Recall number: D-576-2013.