Class III · Low risk
Day Time Cold & Flu
Subpotent Drug: Phenylephrine component is subpotent.
National Drug Code
Is NDC 68016-0023-79 recalled?
Childrens Cetirizine Hydrochloride
Yes — this exact package was recalled
1 FDA recall names the code 68016-0023-79 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 5 mg/5mL
- Form
- Solution · Oral
- Labeler
- Chain Drug Consortium, LLC (Premier Value)
- Type
- Human OTC Drug
- Product code
- 68016-0023
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
- 68016-0177 See recall 1
- 68016-0304 See recall 1
- 68016-0307 See recall 1
- 68016-0308 See recall 1
- 68016-0316 See recall 1
- 68016-0388 See recall 1
Free recall alerts
Know the day your medication is recalled
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