US Drug Recall Register
Class II · Moderate risk Terminated Initiated Mar 16, 2020 (6 years ago)

Ibuprofen 200 mg liquid filled capsules Advil Liqui-Gel Minis, 160 count bottle NDC…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Labeling: Lacks Warning or Rx Legend- Certain lots does not include required safety warning information in the Drug Facts Panel.

What was recalled

Ibuprofen 200 mg liquid filled capsules Advil Liqui-Gel Minis, 160 count bottle NDC 0573-1769-89 NDC 0573-1769-95

Recalling firm
Glaxosmithkline Consumer Healthcare Holdings
NDC code
0573-1769-89
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1066-2020

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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