# Allergy Relief

NDC: 37808-106
Generic name: Cetirizine Hydrochloride
Labeler / Manufacturer: H E B
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20110520

FDA application: ANDA201546

## Active ingredients

- CETIRIZINE HYDROCHLORIDE: 1 mg/mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"37808-106"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=37808-106
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=fdd3f9a0-b4be-498a-b8e0-1a9740399736