Otc - Active Ingredient
Active Ingredient
Ethyl Alcohol 70%
Zoviro Liquid
FDA Label NDC 83814-005
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 83814-005). 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, inactive ingredient, otc - stop use, warnings, otc - when using, 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
Inactive Ingredient
Inactive Ingredient
Water, Carbomer, Glycerin, Aminomethyl propanol, Triethanolamine, Isopropyl myristate, locopheryl acetate, Panthenol, Aloe barbaden-sis leaf extact, Benzophenone-4, Fragrance
Otc - Stop Use
Stop use and ask a doctor if irritation or rash appears and lasts.
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 - 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.
Indications & Usage
Uses
To reduce bacteria on the skin.
* Please review the disclaimer below.
