Active Ingredients
Benzalkonium chloride 0.13%
Sanitizing Alcohol Free Wipes
FDA Label NDC 81244-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Ironcompany.com, Llc for the product Sanitizing Alcohol Free Wipes (NDC 81244-001). 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 ingredients, purpose, uses, warnings, otc - keep out of reach of children, directions, inactive ingredients, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Uses
For hand sanitizing to decrease bacteria on the skin.
Apply topically to the skin to help prevent cross contamination.
Recommended for repeated use.
Dries in seconds.
Warnings
For external use only
May irritate eyes
Keep out of the reach of children unless under adult supervision
Otc - Keep Out Of Reach Of Children
Keep out of the reach of children unless under adult supervision
Directions
Tear V notch on top of plastic bag.
Pull first wipe from the center of roll up through opening of bag.
Thread first wipe through the dispensing nozzle in lid of floor stand or dispenser.
Close dipenser door. Wipe dispensing tension may be adjusted on top of dispenser. Dispenser must be mounted with wipes dispensing up.
Inactive Ingredients
Water (Aqua), Propylene Glycol, Polysorbate 20, Disodium Cocoamphodiacetate, Citric Acid, Disodium EDTA, Potassium Sorbate, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate (Vitamin E), Fragrance.
Package Label.Principal Display Panel
800 CT REFILL, NDC: 81244-001-01
* Please review the disclaimer below.
