Hand Sanitizing Wipes Cloth
FDA Label NDC 69446-220
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Ez Products Of South Florida, Llc for the product Hand Sanitizing Wipes (NDC 69446-220). 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, do not use, stop use and seek medical attention, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Benzalkonium Chloride (BZK) 0.1%
Purpose
Antibacterial
Use
- Decrease bacteria on the skin.
Warnings
For external use only.
When Using This Product
avoid contact with eyes.If contact occurs, rinse thoroughly with water.
Do Not Use
if irritation and redness develop.
Stop Use And Seek Medical Attention
if condition persists for more than 72 hours.
Keep Out Of Reach Of Children.
If swallowed, seek medical attention or contact Poison Control Center.
Directions
1. Locate tear-notch on the side of pouch.
2. Tear straight across to open.
Do not remove wipes roll from pouch.
3. Pull first wipe from center of roll and thread wipe through dispensing nozzle
Other Information
- Dispose of wipe in the proper container.
- Do not flush down the toilet.
Inactive Ingredients
2-Bromo-2-Nitropropane-1,3-Diol, Alcohol,Aloe Barbadensis Leaf Extract, Chamomilla Recutita Flower Extract, Citric Acid, Fragrance, Iodopropynyl Butylcarbamate, Lauryl Glucoside, Phenoxyethanol, Propylene Glycol, Tetrasodium EDTA, Water.
Package Labeling:
Label (Label)
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