OUTLAST LONG-LASTING HAND SANITIZER- alcohol solution 
HEALTHPOINT, LTD

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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OUTLAST Long-Lasting Hand Sanitizer – alcohol solution
Healthpoint, Ltd.

Drug Facts

Active ingredient

Ethyl Alcohol 70% w/w

Purpose

Antiseptic

Use

Antiseptic Handwash to decrease bacteria on the skin.

Warnings

  • Flammable, keep away from fire or flame.
  • For external use only.
  • Do not use in the eyes, ears, and mucous membranes.
  • If case of contact, rinse eyes thoroughly with water.
  • Stop use and ask doctor if irritation and redness develop.
  • Keep out of reach of children.
  • Do not use on children under the age of two.
  • If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Wet hands thoroughly with product.
  • Rub hands together briskly until dry.
  • Supervise children in the use of the product.

Other information

  • Store upright at 20°-25°C (68°-77°F)
  • May discolor certain fabrics.
  • Harmful to wood finishes and plastics.

Inactive Ingredients

Behentrimonium methosulfate, benzalkonium chloride, butylene glycol, cetyl alcohol, chlorhexidine gluconate, ethylhexylglycerin, isopropyl alcohol, phenoxyethanol, polyquaternium-10, PPG-3 myristyl ether, water.

Marketed by: Healthpoint, Ltd.
Ft. Worth, TX 76107
1-800-441-8227
www.outlastgerms.com
Patent No. 6,846,846
(129349-0610)

PRINCIPAL DISPLAY PANEL

WORKS UP TO 6 HOURS!

NDC 0064-1100-59

OutLastTM LONG-LASTING HAND SANITIZER

UP TO 6 HOURS

Fast-Acting, Long-Lasting
No Sticky Feeling!
With Moisturizers

KILLS 99.99% of Germs

2 fl oz (59 ml)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1d616896-figure-01
OUTLAST  LONG-LASTING HAND SANITIZER
ethyl alcohol solution
Product Information
Product TypeHUMAN OTC DRUG LABELItem Code (Source)NDC:0064-1100
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (ALCOHOL) ALCOHOL0.7 g  in 1 g
Inactive Ingredients
Ingredient NameStrength
BENZALKONIUM CHLORIDE 
BUTYLENE GLYCOL 
CETYL ALCOHOL 
CHLORHEXIDINE GLUCONATE 
ETHYLHEXYLGLYCERIN 
ISOPROPYL ALCOHOL 
PHENOXYETHANOL 
WATER 
Product Characteristics
ColorWHITE (WHITE CLEAR) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0064-1100-5950 g in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E06/01/201004/04/2014
Labeler - HEALTHPOINT, LTD (965634504)
Establishment
NameAddressID/FEIBusiness Operations
DPT LABORATORIES, LTD832224526MANUFACTURE(0064-1100)

Revised: 4/2014
Document Id: f2c7ca11-e403-467f-b4e7-30bfb5a2b90b
Set id: df7383bc-d99a-4847-aaa7-78dc632dac9b
Version: 2
Effective Time: 20140404
 
HEALTHPOINT, LTD