Active Ingredient
ALCOHOL
First Hand Sanitizer
FDA Label NDC 74406-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Korea Life Science Co.,ltd for the product First Hand Sanitizer (NDC 74406-001). 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 active ingredient, inactive ingredient, purpose, warnings, keep out of reach of children, uses, directions, 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
glycerin carbomer, green tea extract, aloe extract, mugwort extract, L-menthol, triethanolamine
Purpose
SANITIZER
Warnings
1.Do not use the product on the following areas:
Around the eyes and ears, in the mouth, large body parts and damaged skin(Irritation may occur)
2.If you experience any of the following symptoms, discontinue use of the product immediately and consult a physician or pharmacist.
1) Hypersensitivity symptoms, e.g. rash, erythema, itchiness, and edema
2)Skin irritation symptoms
3.Other precautions
1) For external use only (do not swallow).
2) Avoid contact with eyes. If contact occurs, wash with clean water and consult a doctor or pharmacist.
3)Be careful not to inhale vapors in cases of extended or prolonged use. (Repeating inhaling of large amounts of ethanol vapor may cause irritation of the mucous membranes and headaches).
Keep Out Of Reach Of Children
Keep out of reach of children and go to the hospital immediately if swallowed.
Uses
Disinfection of hands and skin
Directions
Take an appropriate amount on your hands and rub thoroughly to dry.
Package Label.Principal Display Panel
Label (Label)
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