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Drug Facts
The following Structured Product Label (SPL) was submitted to the FDA by Procurement Services Llc for the product Lux Eoi Hand Sanitizing Gel (NDC 74882-007). 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 other, otc - active ingredient, otc - purpose, indications & usage, warnings, otc - do not use, otc - when using, otc - stop use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Drug Facts
Active ingredients
Ethyl Alcohol 70%
Purpose
Antiseptic
Use[s]
Hand sanitizer to help reduce bacteria that potentially
can cause disease. For use when soap and water are not available.
Warnings
For external use only. Flammable.
Keep away from heat or flame.
Do not use
• In children less than 2 months of age
• On open skin wounds
When using this product keep out of eyes, ears, and mouth.
In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs.
These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help
or contact a Poison Control Center right away.
Directions
• Place enough product on hands to cover all surfaces.
Rub hands together until dry.
• Supervise children under 6 years of age when using this
product to avoid swallowing.
Other information
• Store between 15-30C (59-86F)
• Avoid freezing and excessive heat above 40C (104F)
Inactive ingredientswater, carbomer, glycerin,
triethanolamine.
LUX™
EOI
Hand Sanitizing Gel
Helps reduce bacteria that
potentially can cause disease
33.8 FL OZ
(1 Liter)
NDC 74882-007-01
Distributed by
Procurement Services LLC
Nashville, TN 37215
+1 (615) 345-2544
www.luxeoi.com
PRODUCT OF MEXICO
1 Liter Bottle
500 mL Bottle
200mL Bottle
res
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