Data Foundry

Drug recalls 2013

Novartis Lamisil AT Cream — Class III drug recall D-573-2013

Terminated recall by Novartis Consumer Health, reported 2013-06-12, distributed nationwide. Labeling: Incorrect or Missing Lot and/or Expiration date; The Lot and/or Expiration date on the tube may not

Recall numberD-573-2013
Product typeDrug
ClassificationClass III
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmNovartis Consumer Health, Lincoln, NE, United States
Recall initiated2013-02-19
Classified2013-06-06
Reported by FDA2013-06-12
Terminated2014-11-26
DistributedNationwide (US)
Countries outside the USPA
Reason classeslabeling
UPC / GTIN / UDI-DI00300673998124, 00300673998308, 00300673998339, 00300673998421
NDC00067-3998-12, 00067-3998-30, 00067-3998-33, 00067-3998-42
Lot numbers10104979, 10104980, 10104982, 10104983, 10108355, 10108711, 10108712, 10108714, 10109586, 10109588, 10109981, 10111313, 10111316, 10111507, 10111509, 10112072, 10112073, 10113501, 10114223, 10115133, 10115506, 10115619, 10116816, 10117694, 10117695, 10117696, 10117697, 10119643, 10120283, 10120762, 10120763, 10122695, 10122772

Product

Novartis 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; (b) 12 gm (.42 oz), packaged with UPC code: 300673998124 and NDC code: 0067-3998-12; (c) 30 gm (1 oz), packaged with UPC code: 300673998308 and NDC code: 0067-3998-30; (d) 30 gm (1 oz), packaged with UPC code: 300673998339 and NDC code: 0067-3998-33.

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.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-573-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.