OUTLAST LONG-LASTING HAND SANITIZER

Dosage form: solution
Ingredients: ALCOHOL 0.7g in 1g
Labeler: HEALTHPOINT, LTD
NDC Code: 0064-1100

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.

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

Drug Facts

OTC - ACTIVE INGREDIENT

Active Ingredient                                Purpose

Ethyl Alcohol 70% w/w                          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
OUTLAST  LONG-LASTING HAND SANITIZER
ethyl alcohol solution
Product Information
Product TypeHUMAN OTC DRUGItem 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 Description
1NDC:0064-1100-5950 g in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart33306/01/2010
Labeler - HEALTHPOINT, LTD (965634504)
Establishment
NameAddressID/FEIOperations
DPT LABORATORIES, LTD077744035MANUFACTURE

Revised: 07/2010
 
HEALTHPOINT, LTD

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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