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

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

1d616896-figure-01

OUTLAST  LONG-LASTING HAND SANITIZER
ethyl alcohol  solution
Product Information
Product Type HUMAN OTC DRUG NDC Product Code (Source) 0064-1100
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALCOHOL (ALCOHOL) ALCOHOL 0.7 g  in 1 g
Inactive Ingredients
Ingredient Name Strength
BENZALKONIUM CHLORIDE  
BUTYLENE GLYCOL  
CETYL ALCOHOL  
CHLORHEXIDINE GLUCONATE  
ETHYLHEXYLGLYCERIN  
ISOPROPYL ALCOHOL  
PHENOXYETHANOL  
WATER  
Product Characteristics
Color WHITE (WHITE CLEAR) Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0064-1100-59 50 g In 1 BOTTLE, PLASTIC None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333 06/01/2023

Labeler - HEALTHPOINT, LTD (965634504)
Establishment
Name Address ID/FEI Operations
DPT LABORATORIES, LTD 077744035 MANUFACTURE
Revised: 07/2010HEALTHPOINT, LTD