Dosage & Administration
Store between 15°-30°C (59°-89°F)，Awold freezing and excessive heat above 40°C (104°F)
Hand Sanitizer
FDA Label NDC 66875-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Splendid Keen Limited for the product Hand Sanitizer (NDC 66875-001). 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 dosage & administration, inactive ingredient, indications & usage, otc - active ingredient, otc - keep out of reach of children, otc - purpose, warnings, 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
ALOE EXTRACT,GLYCERIN, ISOPROPYL ALCOHOL, ISOPROPYL MYRISTATE, POLYACRYLIC ACID, PROPYLENE GLYCOL, TOCOPHERYL ACETATE, WATER
Indications & Usage
Place enough product on your hands to cover all suraces.Rub hands together until dry.
Otc - Active Ingredient
ALCOHOL
Otc - Keep Out Of Reach Of Children
keep out of reach of children
Otc - Purpose
Disinfection
Sterilization
No Rinseing
Warnings
For external use only, Flamable. Keep away from heat or flame.
Package Label.Principal Display Panel
Label (Label)
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