Active Ingredient
Ethyl Alcohol 70%
Hand Sanitizer
FDA Label NDC 73549-024
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Fortress Expert Co., Ltd for the product Hand Sanitizer (NDC 73549-024). 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, purpose, use, warnings, when using this product, stop use and ask a doctor if, keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Use
■For handwashing to decrease bacteria on the skin.
Warnings
For external use only: hands
Flammable, keep away from fire or flame
When Using This Product
■keep out of eyes.In case of contact with eyes flush thoroughly with water.
■avoid contact with broken skin
■do not inhale or ingest
Stop Use And Ask A Doctor If
■irritation and redness develop
■condition persists for more than 72 hours
Keep Out Of Reach Of Children
Keep out of reach of children.If swallowed, get medical help or contact a poison control center right away.
Directions
■wet hands thoroughly with product and allow to dry without wiping
■for children under 6, use only under adult supervision
■not recommended for infants
Other Information
■do not store above 105°F
■may discolor some fabrics
■harmful to wood finishes and plastics
Inactive Ingredients
Water(Aqua), PEG-40 Hydrogenated Castor Oil, Fragrance(Parfum) , Acrylates/ C10-30Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Aloe Barbadensis Extract, Butylene Glycol, 1,2-Hexanediol, Caprylhydroxamic Acid, Citric Acid, Disodium EDTA, Tocopheryl Acetate, Red 33, Yellow 5
Package Label
73549-024-01 30ml
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