Active Ingredient
Ethyl Alchol 70%
Zoono Ultra Hand Sanitizer Liquid
FDA Label NDC 69221-501
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Zoono Holdings Usa, Llc for the product Zoono Ultra Hand Sanitizer (NDC 69221-501). 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, uses, warnings, when using this product, stop use and ask a doctor if, keep out of reach of children., directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Uses
For personal hand sanitizing and to reduce bacteria on the skin.
Recommended for repeated use.
Warnings
For external use only.
Do not use in the eyes.
When Using This Product
avoid contact with eyes. In case of eye contact flush eyes with water.
Stop Use And Ask A Doctor If
irritation and redness develop.
Keep Out Of Reach Of Children.
If swallowed get medical help or contact a Poison Control Cener right away.
Directions
Apply liberally to the hands and gently rub until dry.
Inactive Ingredients
Alcohol, Benzalkonium chloride, Fragrance, Polysorbate, Silica Complex 3-(Trimethoxysilyl) Propyl Dimethyl Octadecyl Ammonium Chloride, Water
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