# Zyrtec Allergy

NDC: 53209-5001
Generic name: Cetirizine Hydrochloride
Labeler / Manufacturer: Morning Star OTC
Product type: HUMAN OTC DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20250619

FDA application: NDA019835

## 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:"53209-5001"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=53209-5001
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3efa421d-ea70-4b1f-95d0-7c63b6c39580