The Recall Desk

FDA (Drugs) recall action 64372

Novartis Consumer Health recalled 5 products on 2013-06-12

The FDA (Drugs) publishes a recall like this one as 5 separate product records. They share a firm, a date and a cause; this page is all of them in one place, so the scale of the action is visible rather than spread across 5 pages.

Products
5
Announced
2013-06-12
Critical
0
Units
360,660

Why these products were 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.

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..

The agency’s own wording, quoted from the enforcement report.

The unit total adds up the quantities the agency stated for each product. Where a product record gave no figure, or gave a weight rather than a count, it contributes nothing — so the real total is at least this, never less.

States named across these recalls

1–5 of 5

  • LowFDA (Drugs)··2013-06-12

    Novartis Recalls Voltaren Gel Due to Illegible Lot and Expiration Dates

    Novartis Consumer Health is recalling Voltaren Gel because lot and expiration dates on the tubes may be illegible. The FDA classifies this as a Class III recall.

    Product
    Voltaren Gel (diclofenac sodium topical gel) 1%, for topical use only, RX only, a) Packaged in 20 gm tubes, NDC 63481-684-83 (physician sample product) and b) 100 gm tubes, NDC 63481-684-47 (the 100 g tubes are also packaged 3/100-g tubes/packs (UPC code: 363481684030 NDC code…
    Category
    Distribution
    1 state
  • LowFDA (Drugs)··2013-06-12

    Novartis Recalls Target Up & Up Athlete's Foot Cream for Labeling Issues

    Novartis is recalling Target Up & Up athlete's foot cream because the lot and expiration dates on the tubes may not be legible.

    Product
    Target Up & Up, athlete's foot cream, full prescription strength, terbinafine hydrochloride 1% antifungal, 30 g (1 oz), compare to active ingredient in Lamisil, NDC 0067-6382-30 & UPC code: 300676382302 (Novartis) Target NDC 1167-3401-04, Distributed by Target Corp.…
    Category
    Distribution
    1 state
  • LowFDA (Drugs)··2013-06-12

    Novartis Lamisil AT Cream Recalled for Illegible Lot and Expiration Dates

    Novartis is recalling Lamisil AT Cream because the lot and expiration dates on the tubes may be illegible. The recall covers 12-gm and 30-gm tubes distributed nationwide, in Puerto Rico, and in Panama.

    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…
    Category
    Distribution
    1 state
  • LowFDA (Drugs)··2013-06-12

    Novartis Recalls Lamisil AT Cream Due to Illegible Labeling

    Novartis Consumer Health is recalling specific lots of Lamisil AT Cream because the lot and expiration dates on the tubes may be illegible.

    Product
    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
    Category
    Distribution
    1 state
  • LowFDA (Drugs)··2013-06-12

    Novartis Lamisil AT Cream Recalled for Illegible Lot and Expiration Dates

    Novartis is recalling 219,600 tubes of Lamisil AT Cream because the lot and expiration dates may be illegible.

    Product
    Novartis Lamisil AT Cream for Jock Itch (terbinafine hydrochloride 1% antifungal), a) 12 g (.42 oz) Tube, NDC 0067-3999-12, Novartis Consumer Health, Inc., Parsitan, NJ. UPC code: 300673999121, (Vertical Pack) and b) packaged in a horizontal package12 gm (.42 oz) Tube, NDC…
    Category
    Distribution
    1 state