Drug recall D-1323-2020
Product
Gaviscon Regular Strength Liquid Antacid Cool Mint, 12 FL OZ (355 mL), Distributed by: GSK Consumer Healthcare Warren, NJ 07059, NDC 0135-0094-41
Reason for recall
Labeling: Label lacks warning - Magnesium safety warning is not present on the Gaviscon bottle label.
Lots and codes
Lot #: 8H21C1, Exp 7/31/2020; 9B25C1, Exp 1/31/2021; 9D02C1, Exp 2/28/2021; 9G01C1, Exp 5/31/2021
Recall details
- Recalling firm
- Glaxosmithkline Consumer Healthcare Holdings, Warren, NJ
- Quantity
- 151,344 bottles
- Distribution
- U.S.A. Nationwide
- Type
- Voluntary: Firm initiated
- Recall initiated
- May 28, 2020
- Terminated
- January 24, 2022
Related products
- Gaviscon – drug information
- NDC 0135-0094 Gaviscon · Aluminum Hydroxide 95 mg/15mL; Magnesium Carbonate 358… · Haleon US Holdings LLC
- NDC 0135-0095 Gaviscon · Aluminum Hydroxide 254 mg/5mL; Magnesium Carbonate 237.5… · Haleon US Holdings LLC
- NDC 0135-0574 Gaviscon · Aluminum Hydroxide 254 mg/5mL; Magnesium Carbonate 237.5… · Haleon US Holdings LLC