Pure X Disinfecting Wipes
FDA Label NDC 80443-075
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Snapsak Ltd for the product Pure X Disinfecting Wipes (NDC 80443-075). 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 ingredients, purpose, indication and usage, warnings, otc - keep out of reach of children, directions of use, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredients
Ethyl Alcohol 75%
Benzalkonium Chloride 0.10%
Purpose
Antiseptic
Indication And Usage
• For hand washing in order to sanitize skin with a 99.9% efficiency (hands must air dry)
Warnings
• For external use only.
• Keep out of reach of eyes. If contact occurs, rinse thoroughly with water.
• Do not use if you are allergic to any of the ingredients.
• Discontinue use if irritation or redness develops, and if condition persists for more than 72 hours consult a physician.
Otc - Keep Out Of Reach Of Children
• Keep out of reach of children unless under adult supervision.
• If swallowed, get medical help
Directions Of Use
• Wet hands thoroughly with product and allow to dry without rinse.
• Children under six years of age should be supervised when using this product.
Other Information
• Store in a dry place away from fire.
Inactive Ingredients
• Purified (RO) Water, Aloe Vera Extract
Packaging
Image (8044307501 1)
Image (8044307501 2)
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