Otc - Active Ingredient
benzalkonium chloride
Kazu Hand Sanitizer Wipes
FDA Label NDC 76966-0015
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by N Bridge Inc. for the product Kazu Hand Sanitizer Wipes (NDC 76966-0015). 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 otc - active ingredient, inactive ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, 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
Inactive Ingredient
water, glycerin, polysorbate 80, sodium benzoate, benzalkonium chloride, citric acid, maltodextrin, aloe barbadensis leaf juice powder, limonene, tocopheryl acetate, linalool, citral, citronellol, geraniol, benzyl benzoate, benzyl salicylate, farnesol, eugenol, isoeugenol, benzyl alcohol, fragrance
Otc - Purpose
Antiseptic
Otc - Keep Out Of Reach Of Children
keep out of reach of the children
Indications & Usage
Wipe hands thoroughly with product and allow to dry.
Discard wipe in trash. Do not flush.
Warnings
For external use only. Flammable. Keep away from heat or flame.
When using this product keep out of eyes. in case of contact with eyes, flush thoroughly with water.
avoid contact with broken skin.
do not inhale or ingest.
Stop use and ask a doctor if irritation and redness develop. condition persists for more than 72 hours.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Dosage & Administration
for external use only
* Please review the disclaimer below.
