Otc - Active Ingredient
Alcohol
Kazu Hand Sanitizer
FDA Label NDC 76966-0002
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 (NDC 76966-0002). 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, Carbomer, Tromethamine, Green Tea Extract, Aloe Extract
Otc - Purpose
Antiseptic
Otc - Keep Out Of Reach Of Children
keep out of reach of the children
Indications & Usage
wet hands thoroughly with product and allow to dry without wiping
for children under 6, use only under adult supervision
not recommended for infants
Warnings
For external use only. Flammable. Keep away from heat or flame.
Do not use
- in children less than 2 months of age
- on open skin wounds
When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
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
Package Label.Principal Display Panel
1 (Label Kazuhandsanitizerai)
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