DIAL PROFESSIONAL ANTIBACTERIAL HAND SANITIZER  - ethyl alcohol liquid 
The Dial Corporation

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Drug Facts

Active ingredient

Ethyl Alcohol 72%

Purpose

Antibacterial

Uses

hand sanitizer to help reduce bacteria that potentially may cause disease

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.

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 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?

1-877-777-3277

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.

container label

DIAL PROFESSIONAL ANTIBACTERIAL HAND SANITIZER  
ethyl alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54340-107
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M) Alcohol72 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE (UNII: 0Y0NQR2GH1)  
PROPYL ALCOHOL (UNII: 96F264O9SV)  
BEHENTRIMONIUM CHLORIDE (UNII: X7GNG3S47T)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:54340-107-271000 mL in 1 BOTTLE, PLASTIC
2NDC:54340-107-121000 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E12/01/2010
Labeler - The Dial Corporation (070252531)
Establishment
NameAddressID/FEIBusiness Operations
Deb Worldwide Healthcare Inc.205662831manufacture

Revised: 3/2011
Document Id: cbcd58a3-60bb-4d12-9da3-83cb2e150982
Set id: 3bbe5c32-c2b5-43ac-9918-1e6f68594bb9
Version: 3
Effective Time: 20110316
 
The Dial Corporation