DIAL PROFESSIONAL ANTIBACTERIAL HAND SANITIZER- ethyl alcohol liquid

Dial Professional Antibacterial Hand Sanitizer by

Drug Labeling and Warnings

Dial Professional Antibacterial Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by The Dial Corporation, Deb Worldwide Healthcare Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient

Ethyl Alcohol 72%

PURPOSE

Purpose

Antibacterial

INDICATIONS & USAGE

Uses

hand sanitizer to help reduce bacteria that potentially may cause disease

WARNINGS

Warnings

For external use only

Flammable.  Keep away from fire or flame.

When using this product

avoid contact with face, eyes, and broken skin.  If eye contact occurs, flush thoroughly with water and seek medical advice.

Stop use and ask a doctor if

irritation and redness develops

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

DOSAGE & ADMINISTRATION

Directions

pump foam into dry hands, wet thoroughly and rub into skin until dry

Children under 6 years of age should be supervised by an adult when using this product.

INACTIVE INGREDIENT

Inactive ingredients

water, n-propanol, bis-PEG-12 dimethicone, behentrimonium chloride, PEG-200 hydrogenated glyceryl palmate, PEG-7 glyceryl cocoate, coco-glucoside, glyceryl linoleammonium chloride

QUESTIONS

Questions?

1-877-777-3277

PRINCIPAL DISPLAY PANEL

Dial Professional

Antibacterial Hand Sanitizer Fragrance Free Foam

Kills 99.99% of germs instantly

Made in Canada

2010 Distributed by The Dial Corporation/A Henkel Company

Scottsdale, AZ 85255

www.dialprofessional.com

Install with label toward wall

Instalar con etiqueta hacia la pared

US Patent Numbers

5445288, 6082586, patent pending

1 Liter (33.8 Fl Oz)

1 QT 1.8 Fl Oz

Latex and Non-latex compatible

Tested on latex and nitrile gloves.

INGREDIENTS AND APPEARANCE

DIAL PROFESSIONAL ANTIBACTERIAL HAND SANITIZER  
ethyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54340-107
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M)	Alcohol	72 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE (UNII: 0Y0NQR2GH1)
PROPYL ALCOHOL (UNII: 96F264O9SV)
BEHENTRIMONIUM CHLORIDE (UNII: X7GNG3S47T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54340-107-27	1000 mL in 1 BOTTLE, PLASTIC
2	NDC: 54340-107-12	1000 mL in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	12/01/2010

Labeler - The Dial Corporation (070252531)

Establishment
Name	Address	ID/FEI	Business Operations
Deb Worldwide Healthcare Inc.		205662831	manufacture