Class III · Low risk
Cetirizine HCl 10 mg Tablet
Failed Impurity/Degradations Specifications; impurity identified as cetirizine monosaccharide ester
National Drug Code
Is NDC 42507-0458-66 recalled?
All Day Allergy
Yes — this exact package was recalled
1 FDA recall names the code 42507-0458-66 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
- HyVee Inc
- Type
- Human OTC Drug
- Product code
- 42507-0458
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
- 42507-0483 See recall 1
Free recall alerts
Know the day your medication is recalled
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