Class III ยท Low risk
Cetirizine hydrochloride
Labeling: Not Elsewhere classified: Product was relabeled as 90 tablet count product although it was a manufacturer in a box with 30 tablet count tablets.
National Drug Code
Is NDC 50090-5510-03 recalled?
Cetirizine · 1 BOTTLE in 1 CARTON (50090-5510-3) / 90 TABLET, FILM COATED in 1 BOTTLE
Yes — this exact package was recalled
1 FDA recall names the code 50090-5510-03 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
- Cetirizine Hydrochloride
- Strength
- CETIRIZINE HYDROCHLORIDE 10 mg/1
- Form
- Tablet, Film Coated · Oral
- Labeler
- A-S Medication Solutions
- Type
- Human OTC Drug
- Product code
- 50090-5510
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
- 50090-1494 Metformin Hydrochloride 1
- 50090-5313 Acetaminophen 1
- 50090-5350 Acetaminophen 1
Free recall alerts
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