# All Day Allergy Relief

NDC: 59726-129
Generic name: Cetirizine HCl
Labeler / Manufacturer: P & L Development, LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20100901
Marketing ended: 20260901
FDA application: ANDA078780

## 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:"59726-129"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=59726-129
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a042d98d-35ad-4d40-8b27-79dafd028096