Zorari Waterless Disinfection
FDA Label NDC 75183-010
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Zorin Pharmaceutical Technology (hangzhou) Co Ltd. for the product Zorari Waterless Disinfection (NDC 75183-010). 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 drug facts, active ingredient, purpose, use, warnings, when using this product, stop use and ask a doctor if, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Benzalkonium Chloride ................. 0.13%
Purpose
Antibacterial
Use
Disinfection gel helps decrease bacteria on skin. When water, soap and towel are not available.
Recommended for repeated use.
Warnings
For external use only.
When Using This Product
Do not apply around eyes. Do not use in ears and mouth. In case of contact with eyes, mouth, flush with water.
Stop Use And Ask A Doctor If
- irritation and redness develops and persists for more than 72 hours.
Keep Out Of Reach Of Children.
Children must be supervised in use of this product.
Directions
Squeeze small amount to your palms and thoroughly spread on both hands. Rub into skin until dry.
Other information:
Store at 25℃， At low temperature, turbidity and precipitation may occur.
Inactive Ingredients
Water (Aqua), Polymerized quatermary ammonium sal.Aceticacid. Glycerin, Aloe extract.
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