Otc - Active Ingredient
Alcohol
K-mega Hand Sanitizer
FDA Label NDC 69969-700
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Soriso for the product K-mega Hand Sanitizer (NDC 69969-700). 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
Butylene Glycol
Carbomer
Triethanolamine
Mulberry Root Extract
Aloe Extract
Allantoin
Tea Tree Oil
Otc - Purpose
Antiseptic
Otc - Keep Out Of Reach Of Children
KEEP OUT OF REACH OF THE CHILDREN
Indications & Usage
For the external use only
Warnings
For external use only.
Flammable, keep away from fire or flame.
When using this product keep out of eyes. If contact with eyes occurs, rinse promptly and thoroughly with water.
Stop use and ask a doctor if significant irritation or sensitization develops.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Dosage & Administration
Spraying an appropriate amount on your hands or skin and rub it well to dry.
Package Label.Principal Display Panel
1 (Label)
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