ENMOTION FOAM HIGH FREQUENCY USE- ethyl alcohol solution

enMotion Foam by

Drug Labeling and Warnings

enMotion Foam by is a Otc medication manufactured, distributed, or labeled by Georgia Pacific Consumer Products, Vi-Jon, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Ethyl Alcohol 70% 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

When using this product do not use in or near eyes.

STOP USE

Stop use and ask a 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.

Directions

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

Inactive ingredients

Water, Isopropyl Alcohol, PEG-12 Dimethicone, Glycerin, Hydrolyzed Jojoba Esters, Caprylic/Capric Triglyceride, Panthenol, Isopropyl Myristate, Aloe Barbadensis Leaf Juice, Zostera Marina Extract, Chamomilla Recutita (Matricaria) Extract, Camellia Sinensis Leaf Extract, Avena Sativa (Oat) Kernel Extract, Euterpe Oleracea Fruit Extract, Butylene Glycol, Sodium PCA, Sodium Lactate, Bisabolol, Hydrolyzed Glycosaminoglycans, Urea, Collagen Amino Acids, Lactic Acid, Phenoxyethanol, Citric Acid, Sodium Benzoate, Potassium Sorbate, Acetyl Hexapeptide-49

Rear label text

enMotion Foam Hand Sanitizer Fragrance Free

SKU 42336

Manufactured for Georgia-Pacific Consumer Products LP. Atlanta, GA 30303

Quesitons? Call 1-866-HELLOGP (435-5647)

or visit us online at www.gppro.com

(c) Georgia Pacific Consumer Products LP. All rights reserved.

alcohol permit SDS-MO-15036, DSP-MO-28, DSP-MO-34

42336-1 PRDRevA16 L0015898BA

principal display panel

High Frequency Use Foam Hand Sanitizer

1000 mL (33.8 FL OZ)

INGREDIENTS AND APPEARANCE

ENMOTION FOAM  HIGH FREQUENCY USE
ethyl alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54622-486
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.7 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
PEG-12 DIMETHICONE (UNII: ZEL54N6W95)
GLYCERIN (UNII: PDC6A3C0OX)
HYDROLYZED JOJOBA ESTERS (ACID FORM) (UNII: UDR641JW8W)
GLYCERYL CAPRYLATE/CAPRATE (UNII: G7515SW10N)
PANTHENOL (UNII: WV9CM0O67Z)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ZOSTERA MARINA WHOLE (UNII: 5JFW9Q62HN)
MATRICARIA CHAMOMILLA FLOWERING TOP OIL (UNII: SA8AR2W4ER)
CAMELLIA SINENSIS FLOWER (UNII: 9I2BJY2J17)
AVENA SATIVA WHOLE (UNII: 5P8D0Z74RG)
EUTERPE OLERACEA WHOLE (UNII: Y57H6218HP)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
SODIUM LACTATE (UNII: TU7HW0W0QT)
.BETA.-BISABOLOL (UNII: LP618AV2EA)
HYDROLYZED GLYCOSAMINOGLYCANS (BOVINE; 50000 MW) (UNII: 997385V0VV)
UREA (UNII: 8W8T17847W)
BOVINE TYPE I COLLAGEN (UNII: FHJ3ATL51C)
LACTIC ACID (UNII: 33X04XA5AT)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
SODIUM BENZOATE (UNII: OJ245FE5EU)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
ACETYL HEXAPEPTIDE-49 (UNII: 4055X1S509)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54622-486-01	1000 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	06/09/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/02/2016

Labeler - Georgia Pacific Consumer Products (806142217)

Establishment
Name	Address	ID/FEI	Business Operations
Vi-Jon, Inc.		790752542	manufacture(54622-486)