# Childrens Zyrtec Allergy

NDC: 50580-782
Generic name: Cetirizine Hydrochloride
Labeler / Manufacturer: Kenvue Brands LLC
Product type: HUMAN OTC DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET, ORALLY DISINTEGRATING
Routes: ORAL
Marketing started: 20140120

FDA application: NDA022578

## Active ingredients

- CETIRIZINE HYDROCHLORIDE: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"50580-782"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50580-782
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a1edc2e6-3661-4d7a-884c-709d73cb89e0
