Class II · Moderate risk
children's allergy
Failed Impurities/Degradation Specifications: unknown impurity higher than the specified limit was detected during routine stability testing.
National Drug Code
Is NDC 56062-0106-08 recalled?
Childrens Allergy · 1 BOTTLE in 1 CARTON (56062-106-08) / 120 mL in 1 BOTTLE
Yes — this exact package was recalled
1 FDA recall names the code 56062-0106-08 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 1 mg/mL
- Form
- Solution · Oral
- Labeler
- Publix Super Markets Inc
- Type
- Human OTC Drug
- Product code
- 56062-0106
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
- 56062-0099 See recall 2
- 56062-0266 Magnesium Citrate 2
- 56062-0264 Magnesium Citrate 1
- 56062-0571 See recall 1
- 56062-0847 allergy relief 1
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