Dosage & Administration
store at a temperature below110*F (43°C)
Hand Sanitizer
FDA Label NDC 55415-002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Jiangsu Meifan Biotechnology Co., Ltd. for the product Hand Sanitizer (NDC 55415-002). 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
Water, Hammemelis Virginiana (Witch Hazel) Flower, Leafistilate, Aloe Barbadensis Leaf Juice, Glycerin, Hydroxyethy Cellulose, Tocopheryl Acetate (Vitamin E)
Indications & Usage
Wet hands throughly and rub together until dry.
Otc - Active Ingredient
ETHYL ALCOHOL
Otc - Keep Out Of Reach Of Children
keep out of children
Otc - Purpose
Disinfection
Sterilization
No Rinseing
Warnings
For extermal use only.When using this product avoid contact with eyes.If contact occurs, rinse with water.Stop use and ask a doctor if skin rirtiti or rednessdevelops.Keep out of reach of children in case of accidentalingestion, get medical help or contact a Poison Control Center immeditely.
Package Label.Principal Display Panel
Label (Label)
* Please review the disclaimer below.
