Drug Facts

Active Ingredient:

Ethanol (60% v/v)

Purpose:

Anti-Microbial Hand Sanitizer

Uses

Helps reduce bacteria that potentially can cause disease
Helps prevent cross contamination by hand contact
Recommended for repeated use

Warnings

For external use only
Flammable, keep away from fire, heat, or flame
Keep out of reach of children.

Do not use near eyes • In case of eye contact flush with water for 15 minutes • If irritation persists stop use of product and get medical attention • In case of accidental ingestion seek medical attention or contact a poison control center immediately.

Directions • Use no water or towels • Apply appropriate amount of product to palm of hand • Rub until hands are completely covered • Agitate lightly until dry • Let air dry for 15 seconds • Do not rinse or wipe with towel.

Other Information

Store in a cool dry place below 104° F.

Inactive Ingredients

Water, Carbomer, Triethanolamine, PEG-75 Lanolin, Aloe Vera Gel, Fragrance.

Bottle Label
HUSKY®
515
INSTANT HAND
SANITIZER
(GEL-TYPE)

Enhanced with Moisturizers
Kills disease causing germs within seconds
Effective against MRSA, VRE, E. coli (0157:H7) Staphylococcus, Streptococcus and other organisms
Assists with OSHA Bloodborne Pathogen Standard Compliance

For Hospital and Professional Use Only
See Drug Facts panel for additional information.

Bag Label
HUSKY®
515
INSTANT HAND
SANITIZER
(GEL-TYPE)

Enhanced with Moisturizers
Kills disease causing germs within seconds
Effective against MRSA, VRE, E. coli (0157:H7) Staphylococcus, Streptococcus and other organisms
Assists with OSHA Bloodborne Pathogen Standard Compliance

For Hospital and Professional Use Only
See Drug Facts panel for additional information.

Align the half moon ears (round side out) with the slots of the dispenser's lower docking area. Press top and bottom of tube firmly into place.

HUSKY 515 INSTANT HAND SANITIZER
husky 515 gel

Product Information
Product Type	HUMAN OTC DRUG	NDC Product Code (Source)	63779-515
Route of Administration	TOPICAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
alcohol (alcohol)	alcohol	600 mL in 1 L

Inactive Ingredients
Ingredient Name	Strength
water
carbomer homopolymer type c
aloe
trolamine

Product Characteristics
Color		Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	NDC	Package Description	Multilevel Packaging
1	63779-515-05	3.785 L In 1 BOTTLE	None
2	63779-515-15	0.044 L In 1 BOTTLE	None
3	63779-515-27	0.118 L In 1 BOTTLE	None
4	63779-515-62	0.237 L In 1 BOTTLE	None
5	63779-515-80	0.800 L In 1 BAG	None
6	63779-515-88	0.237 L In 1 BOTTLE	None
7	63779-515-89	0.490 L In 1 BOTTLE	None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333	10/28/1998

Labeler - Canberra Corporation (068080621)

Establishment
Name	Address	ID/FEI	Operations
Canberra Corporation		068080621	MANUFACTURE

Revised: 12/2009Canberra Corporation