Class II ยท Moderate risk
Ibuprofen 200 mg liquid filled capsules Advil Liqui-Gel Minis
Labeling: Lacks Warning or Rx Legend- Certain lots does not include required safety warning information in the Drug Facts Panel.
National Drug Code
Is NDC 0573-1769-95 recalled?
Advil
Yes — this exact package was recalled
1 FDA recall names the code 0573-1769-95 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
- Active ingredient
- ibuprofen
- Strength
- IBUPROFEN 200 mg/1
- Form
- Capsule, Liquid Filled · Oral
- Labeler
- Haleon US Holdings LLC
- Type
- Human OTC Drug
- Product code
- 0573-1769
Recalls naming this package
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
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