# childrens allergy relief

NDC: 37808-671
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: 20180518

FDA application: ANDA090254

## Active ingredients

- CETIRIZINE HYDROCHLORIDE: 5 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"37808-671"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=37808-671
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e5e7b796-c175-4122-9474-238e38990337