Active Ingredient
benzalkonium chloride 0.13%
Hand Sanitizer Wipes
FDA Label NDC 71766-003
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Hangzhou Linkeweier Daily Chemicals Co., Ltd. for the product Hand Sanitizer Wipes (NDC 71766-003). 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, warning, otc - keep out of reach of children, directions, inactive ingredient, 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
Antimicrobial
Use
for hand sanitizing to decrease bacteria on the skin.
Warning
Flammable. Keep away from heat and flame.
For External use only.
Do not use in eyes. In case of contact, rinse thoroughly with water.
Stop use & ask doctor if rash/redness or irritation appears/develops
and persist for more than 72 hours.
Otc - Keep Out Of Reach Of Children
Keep out of reach from children except under adult supervision.
If swallowed, get medical help or contact a Poison Control Center
Directions
Slowly peel back label and use one wipe. Reseal, keep closed to
prevent evaporation. Thoroughly wipe hands, allow to dry out rinsing.
Discard after single use
Other information
Do not flush down toilet.
Keep away from sunlight.
Store at room temperature 20°-25°Celsius (68°-77° Fahrenheit)
May discolor certain fabrics
Inactive Ingredient
Aqua, Glycerin, Phenoxyethanol, Benzoic Acid, Polysorbate 20,
Aloe Barbadensis Leaf Juice, Sodium Citrate
Package Label.Principal Display Panel
15 (Label.jpg)
* Please review the disclaimer below.
