HUSKY 515 INSTANT HAND SANITIZER- ethanol gel

HUSKY 515 by

Drug Labeling and Warnings

HUSKY 515 by is a Otc medication manufactured, distributed, or labeled by Canberra Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

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.

PRINCIPAL DISPLAY PANEL

Principal Display Panel

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.

INGREDIENTS AND APPEARANCE

HUSKY 515   INSTANT HAND SANITIZER
ethanol gel

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

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
alcohol (UNII: 3K9958V90M) (alcohol - UNII:3K9958V90M)	alcohol	600 mL  in 1 L

Inactive Ingredients
Ingredient Name	Strength
water (UNII: 059QF0KO0R)
carbomer homopolymer type c (UNII: 4Q93RCW27E)
aloe (UNII: V5VD430YW9)
trolamine (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63779-515-05	3.785 L in 1 BOTTLE
2	NDC: 63779-515-15	0.044 L in 1 BOTTLE
3	NDC: 63779-515-27	0.118 L in 1 BOTTLE
4	NDC: 63779-515-62	0.237 L in 1 BOTTLE
5	NDC: 63779-515-80	0.800 L in 1 BAG
6	NDC: 63779-515-88	0.237 L in 1 BOTTLE
7	NDC: 63779-515-89	0.490 L in 1 BOTTLE
8	NDC: 63779-515-20	1.100 L in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	10/28/1998

Labeler - Canberra Corporation (068080621)

Establishment
Name	Address	ID/FEI	Business Operations
Canberra Corporation		068080621	MANUFACTURE