Uses:
To decrease bacteria on skin.
United Airlines Liquid
FDA Label NDC 52305-601
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 52305-601). 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:, inactive ingredients:, drug facts:, purpose:, product / brand name label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Warnings:
For external use only.
Do not use in eyes.
In cse of contact, rinse eyes thoroughly with water.
Stop use and ask a doctor is skin irritation develops.
If ingested, get medical help or contact a Poison Control Center immediately.
Keep out of reach of children.
Directions
Liberally apply product to skin by gently massaging until absorbed.
Supervise children in the use of this product.
Other Information:
Avoid extreme temperatures.
Inactive Ingredients:
Water (Aqua), Glycerin, PEG-40 Hydrogenated Castor Oil, DMDM Hydantoin, Propylene Glycol, Parfum, Aloe Barbadensis Leaf Extract
Drug Facts:
Active Ingredients: Benzalkonium Chloride 0.13%
Purpose:
Antibacterial.
Product / Brand Name Label
Front Label
This product is a hand sanitizer liquid pump. There is no dosage. But typically a passenger will use 1-2 pumps.
* Please review the disclaimer below.
