LUX EOI HAND SANITIZING GEL- ethyl alcohol gel

Lux Eoi Hand Sanitizing Gel by

Drug Labeling and Warnings

Lux Eoi Hand Sanitizing Gel by is a Otc medication manufactured, distributed, or labeled by Procurement Services LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

ACTIVE INGREDIENT

Active ingredients

Ethyl Alcohol 70%

PURPOSE

Purpose

Antiseptic

INDICATIONS & USAGE

Use[s]
Hand sanitizer to help reduce bacteria that potentially
can cause disease. For use when soap and water are not available.

WARNINGS

Warnings
For external use only. Flammable.
Keep away from heat or flame.

DO NOT USE

Do not use
In children less than 2 months of age
On open skin wounds

WHEN USING

When using this product keep out of eyes, ears, and mouth.
In case of contact with eyes, rinse eyes thoroughly with water.

STOP USE

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

Keep out of reach of children. If swallowed, get medical help
or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

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 SAFETY INFORMATION

Other information
Store between 15-30C (59-86F)
Avoid freezing and excessive heat above 40C (104F)

INACTIVE INGREDIENT

Inactive ingredientswater, carbomer, glycerin,
triethanolamine.

Package Labeling

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

INGREDIENTS AND APPEARANCE

LUX EOI HAND SANITIZING GEL 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74882-007
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
GLYCERIN (UNII: PDC6A3C0OX)
TROLAMINE (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74882-007-01	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/17/2020
2	NDC: 74882-007-02	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/17/2020
3	NDC: 74882-007-03	200 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/17/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/17/2020

Labeler - Procurement Services LLC (117471256)

Registrant - Procurement Services LLC (117471256)