Class III ยท Low risk
Advil PM Caplets
Subpotent Drug: This lot is being recalled because of out-of-specification test results for Diphenhydramine citrate.
National Drug Code
Is NDC 0573-0164-43 recalled?
Advil Pm · 1 BOTTLE in 1 CARTON (0573-0164-43) / 120 TABLET, COATED in 1 BOTTLE
Yes — this exact package was recalled
1 FDA recall names the code 0573-0164-43 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
- diphenhydramine citrate and ibuprofen
- Strength
- DIPHENHYDRAMINE CITRATE 38 mg/1; IBUPROFEN 200 mg/1
- Form
- Tablet, Coated · Oral
- Labeler
- Haleon US Holdings LLC
- Type
- Human OTC Drug
- Product code
- 0573-0164
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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