ENMOTION FOAM HAND SANITIZER- ethyl alcohol liquid

EnMotion Foam Hand Sanitizer by

Drug Labeling and Warnings

EnMotion Foam Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Georgia-Pacific Consumer Products LP. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

ACTIVE INGREDIENT

Active ingredient

Ethyl Alcohol 70% v/v

PURPOSE

Purpose

Antiseptic

INDICATIONS & USAGE

Uses

• To decrease bacteria on skin that could cause disease
• Recommended for repeated use

WARNINGS

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 and ask doctor 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.

DOSAGE & ADMINISTRATION

Directions

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

INACTIVE INGREDIENT

Inactive ingredients Water (Aqua), Isopropyl Alcohol, PEG-12 Dimethicone, Glycerin, Hydrolyzed Jojoba Esters, Caprylic/Capric Triglyceride, Panthenol, Isopropyl Myristate, Aloe Barbadensis Leaf Juice, FD&C Blue #1, FD&C Yellow #5

SPL UNCLASSIFIED SECTION

Manufactured in US of domestic and foreign raw materials.

©2018 GP PRO. All rights reserved.

Unless otherwise noted, all trademarks are owned or licensed to Georgia-Pacific Consumer Products.

Contact Georgia-Pacific at 1-866-HELLOGP (1-866-435-5647) or visit: www.gppro.com

SPL UNCLASSIFIED SECTION

Alcohol Permit SDS-KY-15002

NSF Nonfood Compounds Program Listed E3 Registration 152100

Manufactured for Georgia-Pacific Professional

Atlanta, GA 30303

PRINCIPAL DISPLAY PANEL

enMotion
E3 Rated-Foam Hand Sanitizer
Fragrance Free, Light Green
2-1000 mL (33.8 FL OZ)
TOTAL: 2000 mL (67.6 FL OZ)

INGREDIENTS AND APPEARANCE

ENMOTION FOAM HAND SANITIZER 
ethyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54622-120
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)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
PEG-12 DIMETHICONE (300 CST) (UNII: ZEL54N6W95)
GLYCERIN (UNII: PDC6A3C0OX)
POTASSIUM HYDROLYZED JOJOBA ESTERS (UNII: CH428W5O62)
PANTHENOL (UNII: WV9CM0O67Z)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54622-120-01	2 in 1 BOX	01/25/2018
1		1000 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	01/25/2018

Labeler - Georgia-Pacific Consumer Products (806142217)