Active Ingredient
Benzalkonium Chloride 0.12% w/w.
Viroclear
FDA Label NDC 81909-0001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Bioinnovate Pty Ltd for the product Viroclear (NDC 81909-0001). 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, 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, Hand Sanitizer
Uses
- Hand sanitizer to decrease bacteria on the skin.
- For use when soap and water are not available.
Warnings
For external use only.
When Using This Product
When using this product, keep out of eyes, ears and mouth. In case ofcontact with eyes, rinse eyes thoroughly with water.
Stop Use And Ask A Doctor
Discontinue use if irritation and redness develops.
Keep Out Of Reach Of Children
In case of accidental ingestion, seek medical attention or contact a poison control centre immediately.
Directions
Apply 2-3 sprays onto dry hands and rub hands together vigorously.
Other Information
Store in a cool dry place below 104° F.
Inactive Ingredients
Water/Aqua, Leptospermum Petersonii (Lemon Bush) Leaf Extract, Matricaria Chamomilla (Chamomile) Flower Extract.
Questions Or Comments
Call +1 905 542 2900
Package Label - Principal Display Panel
50 mL; NDC 81909-0001-1
* Please review the disclaimer below.
