Glaxosmithkline Consumer Healthcare Holdings recalls Ibuprofen 200 mg liquid filled capsules Advil Liqui-Gel Minis, 160 count bottle NDC 0573-1769-89 NDC 0573-1769-95
Glaxosmithkline recalls 160-count Advil Liqui-Gel Minis 200mg capsules due to missing safety warnings on Drug Facts panel. Consumers should check lot numbers and contact for details.
Lower-risk recall
Labeling: Lacks Warning or Rx Legend- Certain lots does not include required safety warning information in the Drug Facts Panel.
Contact the company & request your remedy
What happened, in plain English
Glaxosmithkline is recalling 160-count Advil Liqui-Gel Minis 200mg liquid capsules because certain batches lack required safety warnings on the label. This could lead to improper use if consumers don't see the warning information. Read more at govinfonow.com/recall/37307-glaxosmithkline-advil-liqui-gel-minis-200mg-capsules-lack-safety-warning.
Source Summary by GovInfoNow · govinfonow.com/recall/37307-glaxosmithkline-advil-liqui-gel-minis-200mg-capsules-lack-safety-warning · Updated October 5, 2026 · FDA enforcement record: FDA #D-1066-2020
Cite this page
“Glaxosmithkline Advil Liqui-Gel Minis 200mg Capsules Lack Safety Warning.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/37307-glaxosmithkline-advil-liqui-gel-minis-200mg-capsules-lack-safety-warning. Based on FDA recall #D-1066-2020 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1066-2020%22&limit=1).
Why it’s dangerous
The capsules lack required safety warnings in the Drug Facts panel, which could mean users don't see important information about potential risks like stomach issues or interactions with other medications. This is a labeling issue, not a physical defect in the product.
Who’s affected
People who own or use the recalled Advil Liqui-Gel Minis 200mg capsules with specific lot numbers are affected. Those who take ibuprofen regularly without checking the label may be at risk of missing safety information.
How to tell if you have this one
Check for lot numbers R53074 through R62780 on the bottle, which were sold between October 2020 and June 2021. The product is a 160-count bottle of Advil Liqui-Gel Minis 200mg liquid capsules.
- Brand
Glaxosmithkline- Category
Drug
All 5 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class II- Status
Terminated- Distribution
Product was distributed throughout the United States, including Puerto Rico.
| Recall number | Product, codes & lots | Quantity | NDC |
|---|---|---|---|
| D-1065-2020 | Ibuprofen 200 mg Chlorpheniramine Maleate 4mg Phenylephrine 10 mg tablets. Advil Allergy & Congestion Relief 10 and 20 count blister tray in carton NDC 0573-0196-10, item # F00573019610C, 10 ct. blister NDC 0573-0196-20, item # F00573019620C, 20 ct. blister NDC 0573-0196-10, item # F00573019610R, 10 ct. blister; Batch/Lot Numbers: R73995, exp. date 07/31/2021 R53915, exp. date 05/31/2020 9324HA, exp. date 07/31/2021 9327HA, exp. date 07/31/2021 | 471,024 blisters | 0573-0196-01, 0573-0196-10, 0573-0196-20, 0573-0196-02, 0573-2161-03, 0057301961, 0057301962 |
| D-1066-2020 | Ibuprofen 200 mg liquid filled capsules Advil Liqui-Gel Minis, 160 count bottle NDC 0573-1769-89 NDC 0573-1769-95; 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. | 446,628 bottles | 0573-0169-17, 0573-0169-02, 0573-0169-19, 0573-0169-20, 0573-0169-40, 0573-0169-11, 0573-0169-89, 0573-0169-30, 0573-0169-31, 0573-0169-86, 0573-0169-51, 0573-0169-43, 0573-0169-49, 0573-0169-52, 0573-0169-08, 0573-0169-22, 0573-0169-13, 0573-0169-76, 0573-0169-16, 0573-0149-13, 0573-0149-04, 0573-0149-66, 0573-0149-91, 0573-1769-20, 0573-1769-80, 0573-1769-89, 0573-1769-14, 0573-1769-13, 0573-1769-09, 0573-1769-02, 0573-1769-87, 0573-1769-16, 0573-1769-31, 0573-1769-92, 0573-1769-95, 0057317698 |
| D-1067-2020 | Ibuprofen 50 mg per 1.25 mL Oral Suspension Advil Infant Concentrated Drops White Grape 0.75 oz. and 1 oz. bottles NDC 0573-0191-75 (0.75 oz.) NDC 0573-0191-50 (1 oz.); Batch/Lot # R73761, exp. date 01/31/2021, Item # F00573019175, 0.75 oz. R74936, exp. date 02/28/2021, Item # F00573019175, 0.75 oz. R56290, exp. date 03/31/2020, Item # F00573019150, 1 oz. R60959, exp. date 02/28/2021, Item # F00573019150, 1 oz. R78826, exp. date 11/30/2021, Item # F00573019150, 1 oz. 9335UA, exp. date 01/31/2021, item # F00573019175A - Co-package 9336UA, exp. date 02/28/2021, item # F00573019175A - Co-package | 151,056 bottles | 0573-0191-20, 0573-0191-50, 0573-0191-22, 0573-0191-75, 0057301917, 0057301915 |
| D-1068-2020 | Advil Sinus Congestion and Pain/Advil Allergy and Congestion Relief 8 pc with $1 IRC (mixed product display - only Advil Allergy & Congestion is impacted). NDC # 0573-2161-14 SKU# F00573216114A (original lot # R73995) Co-packaged Batch/Lot # 0045DB, 9327VB, 0017DA & 9353WA; Batch/Lot # 0045DB, exp. date 07/31/2021, original lot # R73995 9327VB, exp. date 07/31/2021, original lot # R73995 0017DA, exp. date 07/31/2021, original lot # R73995 9353WA, exp. date 07/31/2021, original lot # R73995 | 566 blister packs | — |
| D-1069-2020 | Advil Liqui-Gel Mini 160+20+20 CT (e-commerce) NDC # 0573-1715-59 SKU# F00573171559 (original lot # R53074) Co-packaged Batch/Lot # 0198FR & 3188FRB; Batch/Lot # Lot # 0198FR, original lot # R53074, exp. date 10/31/2020 Lot # 3188FRB, original lot # R53074, exp. date 10/31/2020 | 4,104 bottles | — |
What to do — step by step
Check Product Lot Number
Look for lot numbers R53074 through R62780 on the bottle to confirm if it's recalled.
Contact Manufacturer
Reach out to Glaxosmithkline Consumer Healthcare Holdings for further instructions on the recall.
Questions people ask
Why is this product being recalled?
The product lacks required safety warnings in the Drug Facts panel, which could lead to users missing important information about potential risks.
What should I do if I have the recalled product?
Check the lot number on the bottle to see if it's in the recalled range, then contact Glaxosmithkline Consumer Healthcare Holdings for further instructions.
Are there any safety risks from using this product?
The recall is due to missing safety warnings, not a physical defect. However, users might not see important information about potential risks like stomach issues or medication interactions.
Contact Glaxosmithkline
We’ve drafted a message you can send Glaxosmithkline to request your refund or repair — edit it as you like.
Subject: Recall D-1066-2020 — Glaxosmithkline Glaxosmithkline Hello, I own a Glaxosmithkline that is covered by recall D-1066-2020 from Glaxosmithkline. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-1066-2020 (March 16, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1066-2020 to see it in context.
- Plain-language summary written by qwen3:4b on October 5, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.