Class III ยท Low risk
Cetirizine HCl 10 mg Tablet
Failed Impurity/Degradations Specifications; impurity identified as cetirizine monosaccharide ester
National Drug Code
Is NDC 41163-0458-66 recalled?
Equaline all day allergy · 14 BLISTER PACK in 1 CARTON (41163-458-66) / 1 TABLET, FILM COATED in 1 BLISTER PACK
Yes — this exact package was recalled
1 FDA recall names the code 41163-0458-66 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
- United Natural Foods, Inc. dba UNFI
- Type
- Human OTC Drug
- Product code
- 41163-0458
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
- 41163-0769 citroma 2
- 41163-0129 Equaline Extra Strength Assorted Berry Antacid 1
- 41163-0171 EQU Ultra Strength Antacid Assorted Fruit 171AF 1
- 41163-0343 Equaline Nasal 1
- 41163-0404 See recall 1
- 41163-0528 See recall 1
Free recall alerts
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