Dosage & Administration
Keep away from flame or high heat.
Hand Sanitizer
FDA Label NDC 41366-005
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Zhejiang Meimi Technology Co., Ltd. for the product Hand Sanitizer (NDC 41366-005). 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(Aqua, Eau.)
Propylene Glycol
Carbomer
Fragrance (Parfum)
Tocopheryl Acetate
DISODIUM EDTA
Linalool
Indications & Usage
Put enough product in your palm to cover hands and rub hands together briskly until dry Children should be supervised when using Hand Sanitizer.
Otc - Active Ingredient
alcohol
Otc - Keep Out Of Reach Of Children
keep out of children
Otc - Purpose
Disinfection
Sterilization
Warnings
Keep away from flame or high heat.
Package Label.Principal Display Panel
Label (Label)
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