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DRUG FACTS:
Distributed By: Thor Microbials
Hand Sanitizer
FDA Label NDC 80581-087
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Quadsil Inc for the product Hand Sanitizer (NDC 80581-087). 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 other, active ingredient, purpose, inactive ingredients, uses, directions, warnings, otc - 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 0.1%
Purpose
Antimicrobial
Inactive Ingredients
Cyclopentasiloxane, Dimethacone, Crosspolymer, PPG-3, Benzyl Ether Ethylhexanoate, Octadecyldimethyl Trimethoxysilylpropyl Ammonium Chloride.
Uses
For Hand Sanitizing.
Directions
Prime pump, use one pump to cover both hands.
Warnings
The Human Corona Virus is not COVID-19. For External Use Only. Avoid contacts with eyes. In case of eye contact, flush eyes with water. If irritation or redness develops, stop use. If condition persists for more than 72 hours, contact a doctor.
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.
Principal Display Panel - 30 Ml Bottle Label
Si + ARMOR
LONG-LASTING ANTIMICROBIAL
HAND SANITIZER
ALCOHOL FREE
KILLS 99.9% OF GERMS &
HUMAN CORONA VIRUS
4-8 HOURS
OF GERM PROTECTION
Softens Hands • 200 Applications
1 fl oz ( 30 ml)
MADE IN
USA
Principal Display Panel (30 ml Bottle Label)
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