# Zoviro

NDC: 83814-007
Generic name: ALCOHOL
Labeler / Manufacturer: Zoviro, LLC
Product type: HUMAN OTC DRUG
Marketing category: OTC monograph drug
Dosage form: GEL
Routes: TOPICAL
Marketing started: 20260801

FDA application: 505G(a)(3)

## Active ingredients

- ALCOHOL: 70 mL/100mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"83814-007"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=83814-007
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9c8ca084-8aef-4616-8d51-aaff3eb25343