Active Ingredient
Benzalkonium Chloride 0.13% v/v
Hand Sanitizing Wipes
FDA Label NDC 62685-219
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Tropical Degil Cosmetics Industries Ltd for the product Hand Sanitizing Wipes (NDC 62685-219). 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, use, warnings, do not use, otc - when using, otc - ask doctor, 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
Purpose
Hand Sanitizer, Antiseptic
Use
Hand sanitizer to help reduce bacteria on the skin.
Warnings
For external use only
Do Not Use
if you are allergic to any of the ingredients
Otc - When Using
When using this product do not use in or near the eyes. If contact occurs, rinse thoroughly with water.
Otc - Ask Doctor
Stop use and ask a doctor if irritation or redness develops and lasts for more than 72 hours.
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.
Directions
For adults and children 3 years and over, wipe hands and discard. Allow hands to air dry.
Inactive Ingredients
Alcohol Denatured, Aloe Barbadensis Leaf Extract, Benzoic Acid, Caprylyl/Capryl Glucoside, Citric Acid, Dehydroacetic Acid, Disodium EDTA, Fragrance, Glycerin, Phenoxyethanol, Polysorbate 20, Water
Other Safety Information
Other information Store in a cool dry place.
Principal Display Panel
25 wipes. 0.13% Benzalkonium Chloride
* Please review the disclaimer below.
