FDA Drug recall D-1066-2020
Ibuprofen 200 mg liquid filled capsules Advil Liqui-Gel Minis, 160 count bottle NDC 0573-1769-89 NDC 0573-1769-95
- FDA Drug
- Class II
- terminated
- Published 2020-04-01
On 2020-04-01 the FDA classified a Class II recall of Ibuprofen 200 mg liquid filled capsules Advil Liqui-Gel Minis, 160 count bottle NDC 0573-1769-89 NDC 0573-1769-95 by Glaxosmithkline Consumer Healthcare Holdings, citing labeling: Lacks Warning or Rx Legend- Certain lots does not include required safety warning information in the Drug Facts Panel.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-1066-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2020-03-16 |
| Published | 2020-04-01 |
| Last updated | 2026-09-13 11:52 UTC |
| Company | Glaxosmithkline Consumer Healthcare Holdings |
| Distribution | US |
Product
Ibuprofen 200 mg liquid filled capsules Advil Liqui-Gel Minis, 160 count bottle NDC 0573-1769-89 NDC 0573-1769-95
Reason
Labeling: Lacks Warning or Rx Legend- Certain lots does not include required safety warning information in the Drug Facts Panel.
Identifiers
| ndc | 0573-0169-17 |
|---|---|
| ndc | 0573-0169-02 |
| ndc | 0573-0169-19 |
| ndc | 0573-0169-20 |
| ndc | 0573-0169-40 |
| ndc | 0573-0169-11 |
| ndc | 0573-0169-89 |
| ndc | 0573-0169-30 |
| ndc | 0573-0169-31 |
| ndc | 0573-0169-86 |
| ndc | 0573-0169-51 |
| ndc | 0573-0169-43 |
| ndc | 0573-0169-49 |
| ndc | 0573-0169-52 |
| ndc | 0573-0169-08 |
| ndc | 0573-0169-22 |
| ndc | 0573-0169-13 |
| ndc | 0573-0169-76 |
| ndc | 0573-0169-16 |
| ndc | 0573-0149-13 |
| ndc | 0573-0149-04 |
| ndc | 0573-0149-66 |
| ndc | 0573-0149-91 |
| ndc | 0573-1769-20 |
| ndc | 0573-1769-80 |
| ndc | 0573-1769-89 |
| ndc | 0573-1769-14 |
| ndc | 0573-1769-13 |
| ndc | 0573-1769-09 |
| ndc | 0573-1769-02 |
| ndc | 0573-1769-87 |
| ndc | 0573-1769-16 |
| ndc | 0573-1769-31 |
| ndc | 0573-1769-92 |
| ndc | 0573-1769-95 |
| ndc | 0057317698 |
| code_info | Batch/Lot Numbers: R53074, exp. date 10/31/2020, item # F00573176989, 160 ct. R53075, exp. date 10/31/2020, item # F…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. |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1066-2020%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.