Active Ingredient
Benzalkonium chloride 0.12%
Zoviro Liquid
FDA Label NDC 83814-006
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 83814-006). 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 active ingredient, purpose, use, warnings, when using this product, keep out of reach of children & pets, directions, inactive ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Use
Hand sanitizer to help reduce bacteria that potentially can cause disease.
Warnings
For external use only
When Using This Product
avoid contact with eyes. In case of eye contact, rinse with water.
Keep Out Of Reach Of Children & Pets
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Pump a small amount into your palm. Rub hands together briskly until dry.
No rinsing required.
Inactive Ingredient
Water, Propanediol, Glycerin, Polysorbate 20, Decyl Glucoside, Cetylpyridinium Chloride, Butylene Glycol, Sodium Citrate, Citric Acid, Hydroxyacetophenone, 1,2-Hexanediol, Citrus Paradisi (Grapefruit) Peel Oil, Citrus Junos Fruit Oil, Portulaca Oleracea Extract, Chrysanthellum Indicum Extract, Pelargonium Graveolens Flower/Leaf/Stem Extract, Mentha Arvensis Leaf Extract, Aloe Barbadensis Extract, Sophora Angustifolia Root Extract, Panthenol
* Please review the disclaimer below.
