Reported Jun 12, 2013 · Terminated

Novartis Lamisil AT Cream, Terbinafine Hydrochloride Cream 1% Antifungal, Novartis Consumer Health, Inc., Parsippany,…

Novartis Consumer Health

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Novartis Consumer Health · 10401 Hwy 6 · Lincoln, NE · 68517-9626

Is this the product you have?

4 of 4 products

Products covered by this recall
#BarcodesProduct as published
1300673998421Novartis Lamisil AT Cream, Terbinafine Hydrochloride Cream 1% Antifungal, Novartis Consumer Health, Inc., Parsippany, NJ. (a)12 gm (.42 oz), packaged with UPC code 300673998421 and NDC code: 0067-3998-42
2300673998124(b) 12 gm (.42 oz), packaged with UPC code: 300673998124 and NDC code: 0067-3998-12
3300673998308(c) 30 gm (1 oz), packaged with UPC code: 300673998308 and NDC code: 0067-3998-30
4300673998339(d) 30 gm (1 oz), packaged with UPC code: 300673998339 and NDC code: 0067-3998-33.
Lot codes and dates
  • (12
  • gm) Lot numbers and Exp dates
    • 10109586 30-Apr-2013
    • 10116816 31 May 2013
    • 10117695 31-Jul-2013
    • 10120283 31-Aug-2013
    • 10104980 28-Feb-2013
    • 10108711 31-Mar-2013
    • 10111313 30-Apr-2013
    • 10111509 30-Apr-2013
    • 10115506 30-Jun-2013
    • 10117696 30-Jun-2013
    • 10120763 31-Aug-2013
    • 10122695 30-Sep-2013
    • 10104983 28-Feb-2013
    • 10108714 31-Mar-2013
    • 10119643 31-Jul-2013 (30
  • gm) Lot numbers and Exp dates
    • 10104979
    • 28-Feb-2013
    • 10108712
    • 31-Mar-2013
    • 10109588
    • 30-Apr-2013
    • 10111507
    • 30-Apr-2013
    • 10115133
    • 31-May-2013
    • 10115619
    • 30-Jun-2013
    • 10117694
    • 31-Aug-2013
    • 10120762
    • 30-Sep-2013
    • 10109981
    • 31-Mar-2013
    • 10111316
    • 31-Mar-2013
    • 10114223
    • 31-May-2013
    • 10117697
    • 30-Jun-2013
    • 10104982
    • 28-Feb-2013
    • 10108355
    31-Mar-2013, 10112072 30-Apr-2013, 10112073 30-Apr-2013 10113501 31-May-2013, 10122772 31-Aug-2013
Amount recalled
818,064 (12-gm) tubes and 836,376 (30-gm) tubes

This recall covers 5 products

The agency filed one notice per product. You are reading one of them; the other 4 are below.

Where it was sold

  • Nationwide
  • PR

Why it was 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.

This product is unlikely to cause harm, but it breaks a safety or labelling rule.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA drug enforcement) notice

Notice updated Nov 26, 2014 · Data as of Sep 19, 6:30 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.