Drug recall D-1066-2020
Product
Ibuprofen 200 mg liquid filled capsules Advil Liqui-Gel Minis, 160 count bottle NDC 0573-1769-89 NDC 0573-1769-95
Reason for recall
Labeling: Lacks Warning or Rx Legend- Certain lots does not include required safety warning information in the Drug Facts Panel.
Lots and codes
Batch/Lot Numbers: R53074, exp. date 10/31/2020, item # F00573176989, 160 ct. R53075, exp. date 10/31/2020, item # F00573176989, 160 ct. R53076, exp. date 11/30/2020, item # F00573176989, 160 ct. R53077, exp. date 11/30/2020, item # F00573176989, 160 ct. R53081, exp. date 11/30/2020, item # F00573176989, 160 ct. R53901, exp. date 02/28/2021, item # F00573176989, 160 ct. R53902, exp. date 03/31/2021, item # F00573176989, 160 ct. R62780, exp. date 06/30/2021, item # F00573176989, 160 ct.
Recall details
- Recalling firm
- Glaxosmithkline Consumer Healthcare Holdings, Warren, NJ
- Quantity
- 446,628 bottles
- Distribution
- Product was distributed throughout the United States, including Puerto Rico.
- Type
- Voluntary: Firm initiated
- Recall initiated
- March 16, 2020
- Terminated
- October 28, 2021
Related products
- Advil – drug information
- NDC 0573-1769 Advil · Ibuprofen 200 mg/1 · Haleon US Holdings LLC
- NDC 0573-0149 Advil · Ibuprofen 200 mg/1 · Haleon US Holdings LLC
- NDC 0573-0169 Advil · Ibuprofen 200 mg/1 · Haleon US Holdings LLC