Otc - Active Ingredient
Active ingredient
Ethyl Alcohol 70%
Zoviro Gel
FDA Label NDC 83814-007
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Zoviro, Llc for the product Zoviro (NDC 83814-007). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding otc - active ingredient, otc - purpose, indications & usage, warnings, otc - when using, otc - stop use, otc - keep out of reach of children, dosage & administration, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Purpose
Antimicrobial
Indications & Usage
Uses
To reduce bacteria on the skin.
Warnings
Warnings
Flammable. Keep away from fire or flame.
For external use only.
Otc - When Using
When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.
Otc - Stop Use
Stop use and ask a doctor if irritation or rash appears and lasts.
Otc - 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.
Dosage & Administration
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.
How Supplied
Other information
Store below 110°F (43°C).
May discolor certain fabrics or surfaces.
Inactive Ingredient
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.
Package Label.Principal Display Panel
Product label
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