Maalox Nighttime Antacid with Acid Reflux Barrier (calcium carbonate and alginic acid) chewable tablets, 500 mg/200 mg, Mint flavor, 65-count tablets per bottle, Novartis Consumer Health Canada Inc., Mississauga, ON L5N 2X7, foreign labeling containing English and French, NPN 80000899, UPC 0 58478 10091 3.
Reported: August 28, 2013 Initiated: August 6, 2013 #D-909-2013
Product Description
Maalox Nighttime Antacid with Acid Reflux Barrier (calcium carbonate and alginic acid) chewable tablets, 500 mg/200 mg, Mint flavor, 65-count tablets per bottle, Novartis Consumer Health Canada Inc., Mississauga, ON L5N 2X7, foreign labeling containing English and French, NPN 80000899, UPC 0 58478 10091 3.
Reason for Recall
Labeling: Incorrect Or Missing Lot and/or Exp Date: The lot number and/or expiration date may be illegible on the outer plastic bottle packaging.
Details
- Recalling Firm
- Novartis Consumer Health
- Units Affected
- 23,856 bottles
- Distribution
- Nationwide, Canada, and Panama.
- Location
- Lincoln, NE
Frequently Asked Questions
What product was recalled? ▼
Maalox Nighttime Antacid with Acid Reflux Barrier (calcium carbonate and alginic acid) chewable tablets, 500 mg/200 mg, Mint flavor, 65-count tablets per bottle, Novartis Consumer Health Canada Inc., Mississauga, ON L5N 2X7, foreign labeling containing English and French, NPN 80000899, UPC 0 58478 10091 3.. Recalled by Novartis Consumer Health. Units affected: 23,856 bottles.
Why was this product recalled? ▼
Labeling: Incorrect Or Missing Lot and/or Exp Date: The lot number and/or expiration date may be illegible on the outer plastic bottle packaging.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on August 28, 2013. Severity: Low. Recall number: D-909-2013.
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