ENMOTION E3 RATED GEL HAND SANITIZER WITH MOISTURIZERS FRAGRANCE FREE, DYE FREE- ethyl alcohol liquid

enMotion E3 Rated Gel Hand Sanitizer With Moisturizers Fragrance Free, Dye Free by

Drug Labeling and Warnings

enMotion E3 Rated Gel Hand Sanitizer With Moisturizers Fragrance Free, Dye Free by is a Otc medication manufactured, distributed, or labeled by Georgia-Pacific Consumer Products, CYAN Labs S.A. de C.V.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

Ethyl alcohol, 67% v/v

Purpose

Antiseptic

Uses

• To decrease bacteria on skin that could cause disease

• Recommended for repeated use

Warnings

• FLAMMABLE, keep away from fire or flame
• For external use only

When using this product

Do not use in or near eyes. 

Stop use

if irritation or redness develops. If condition persists for more than 72 hours consult a doctor.

Keep out of reach of children.

If swallowed, seek immediate medical attention or call a poison control center.

Directions

Wet hands thoroughly with product and allow to dry without wiping.

Inactive ingredients

Water (Aqua), Isopropyl Alcohol, Aloe Barbadensis Leaf Juice, Carbomer, Diisoprylamine, Glycerin, Isopropyl Myristate, Tocopheryl Acetate.

PRINCIPAL DISPLAY PANEL

enMotion®
E3 Rated Gel Hand Sanitizer with Moisturizers
Fragrance Free, Dye Free
E3 Classificado GelSanitizante y Humectante Para
Manos Sin Fragrancia, Sin Colorantes
2-950mL (32.1 FL OZ)
TOTAL: 1900mL (64.2 FL OZ)
Made in Mexico
enMotion® is a trademark of Georgia-Pacific Consumer Products LP.
Contact Georgia-Pacific at 1-866-HELLOGP(1-866-435-5647)or visit: www.gppro.com

INGREDIENTS AND APPEARANCE

ENMOTION E3 RATED GEL HAND SANITIZER WITH MOISTURIZERS FRAGRANCE FREE, DYE FREE 
ethyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54622-307
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	67 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
SODIUM BENZOATE (UNII: OJ245FE5EU)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
SODIUM SULFITE (UNII: VTK01UQK3G)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
DIISOPROPYLAMINE (UNII: BR9JLI40NO)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
GLYCERIN (UNII: PDC6A3C0OX)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54622-307-01	2 in 1 BOX	04/25/2017
1		950 mL in 1 BAG; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	04/25/2017

Labeler - Georgia-Pacific Consumer Products (806142217)

Registrant - CYAN Labs S.A. de C.V. (812754130)

Establishment
Name	Address	ID/FEI	Business Operations
CYAN Labs S.A. de C.V.		812754130	manufacture(54622-307) , label(54622-307) , pack(54622-307)