# Up and Up Allergy Relief

NDC: 11673-502
Generic name: Cetirizine Hydrochloride
Labeler / Manufacturer: Target Corporation
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20141217

FDA application: ANDA078336

## 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:"11673-502"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=11673-502
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ce93ca5b-2a65-4873-9686-926c44076c6c