Zoviro
Benzalkonium Chloride · Swab · Topical
Active ingredient
Active ingredient Ethyl Alcohol 70%
Purpose
Purpose Antimicrobial
Uses
Uses To reduce bacteria on the skin.
Warnings
Warnings Flammable. Keep away from fire or flame. For external use only.
When using this product
When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.
Stop use and ask a doctor
Stop use and ask a doctor if irritation or rash appears and lasts.
Keep out of reach of children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Directions Place enough product in your palm then rub hands until dry. Children under 6 years of age should be supervised when using this product. Not recommended for infants.
Inactive ingredients
Inactive ingredients Aqua/Water, Glycerin, Propylene Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Lavandula Angustifolia (Lavender) Oil, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, Denatonium Benzoate, Eucalyptus Globulus Leaf Oil.
Label text from the FDA structured product label by Zoviro, LLC (revised Aug 12, 2026). Long sections are shortened; the complete label is on DailyMed.
Active ingredients
- Benzalkonium Chloride in 4 products
- Alcohol in 2 products
Zoviro NDC products (6)
| NDC | Strength & form | Labeler | Type |
|---|---|---|---|
| 83814-001 | Benzalkonium Chloride .13 g/100g Swab | Zoviro, LLC | OTC MONOGRAPH DRUG |
| 83814-003 | Benzalkonium Chloride .13 g/100g Swab | Zoviro, LLC | OTC MONOGRAPH DRUG |
| 83814-004 | Benzalkonium Chloride .13 g/100g Swab | Zoviro, LLC | OTC MONOGRAPH DRUG |
| 83814-005 | Alcohol 70 mL/100mL Liquid | Zoviro, LLC | OTC MONOGRAPH DRUG |
| 83814-006 | Benzalkonium Chloride .12 g/100mL Liquid | Zoviro, LLC | OTC MONOGRAPH DRUG |
| 83814-007 | Alcohol 70 mL/100mL Gel | Zoviro, LLC | OTC MONOGRAPH DRUG |
Frequently asked questions
What is Zoviro used for?
Uses To reduce bacteria on the skin.
Who makes Zoviro?
Zoviro is listed by 1 labeler in the FDA NDC directory, including Zoviro, LLC.