Uses:
To decrease bacteria on the skin that could cause disease. Recommended for repeated use.
United Airlines
FDA Label NDC 52305-223
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Freshorize Ltd. for the product United Airlines (NDC 52305-223). 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 uses:, warnings:, directions:, other information:, drug facts, purpose, inactive ingredients:, brand label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Warnings:
Flammable - Keep away from fire or flame
For external use only.
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 doctor is rash or irritation develops and lasts more than 72 hours.
If product is swallowed, get medical help or contact a Poison Control Center right away.
Keep out of the reach of children.
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°
May discolor some fabrics
Harmful to wood finish and plastics.
Drug Facts
Active ingredient: Ethyl Alcohol 62%
Purpose
Antiseptic
Inactive Ingredients:
Water, Isopropyl Alcohol, Tocopheryl Acetate, Glycerin, Propylene Glycol, Isopropyl Myristate, Carbomer, Aminomethyl Propanol
Front Label
Requires no water or towels.
Apply small amount to hands and rub lightly until dry.
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