HUSKY 575 FOAMING ANTISEPTIC HAND CLEANER- triclosan liquid

HUSKY 575 Foaming Antiseptic Hand Cleaner by

Drug Labeling and Warnings

HUSKY 575 Foaming Antiseptic Hand Cleaner 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:

Triclosan (0.35%)

Purpose:

Antiseptic Hand Cleanser

Uses

• Handwash to help reduce bacteria that potentially can cause disease.
• Recommended for repeated use.

Warnings

• For external use only

• Do not use near eyes

• Keep out of reach of children.

Discontinue use if irritation and redness develop. If condition persists more than 72 hours, consult a doctor.

In case of eye contact flush with water for 15 minutes. If irritation persists, get medical attention

• In case of accidental ingestion, seek medical attention or contact a poison control center immediately.

Directions

• Wet hands and forearms
• Apply appropriate amount (palmful) to hands and forearms
• Scrub hands and forearms thoroughly for 60 seconds
• Use scrub and/or nail brush to aid in cleaning.
• Rinse well
• Wipe dry with towel, repeat if necessary.

Other Information

• Assists with OSHA bloodborne pathogen standard compliance

Inactive Ingredients

Water, Sodium Laureth Sulfate, Sodium Lauryl Sulfate, Propylene Glycol, Lauramide DEA, Cocamide DEA, Cocamidopropyl betaine, Sodium Cumene Sulfonate, Citric Acid, Fragrance, DMDM Hydantoin, Sodium Chloride, FD&C Green #3.

Principal Display Panel

Bottle Label:

HUSKY®

575

FOAMING ANTISEPTIC HAND CLEANER

A Powerful Antiseptic Cleanser for Handwashing

Enhanced with Moisturizers

• Reduces Bacteria on Skin That Can Potentially Cause Disease
• Assists with OSHA Bloodborne Pathogen Standard Compliance

KEEP OUT OF REACH OF CHILDREN

CAUTION

See Drug Facts panel for additional information.

INGREDIENTS AND APPEARANCE

HUSKY 575 FOAMING ANTISEPTIC HAND CLEANER 
triclosan liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63779-575
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
triclosan (UNII: 4NM5039Y5X) (triclosan - UNII:4NM5039Y5X)	triclosan	3.15 g  in 1000 mL

Inactive Ingredients
Ingredient Name	Strength
water (UNII: 059QF0KO0R)
sodium laureth sulfate (UNII: BPV390UAP0)
sodium lauryl sulfate (UNII: 368GB5141J)
propylene glycol (UNII: 6DC9Q167V3)
lauric diethanolamide (UNII: I29I2VHG38)
cocamidopropyl betaine (UNII: 5OCF3O11KX)
coco diethanolamide (UNII: 92005F972D)
citric acid monohydrate (UNII: 2968PHW8QP)
dmdm hydantoin (UNII: BYR0546TOW)
sodium chloride (UNII: 451W47IQ8X)
FD&C Green NO. 3 (UNII: 3P3ONR6O1S)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63779-575-05	3785 mL in 1 BOTTLE
2	NDC: 63779-575-42	50 mL in 1 BOTTLE
3	NDC: 63779-575-20	1100 mL in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	10/11/2010

Labeler - Canberra Corporation (068080621)

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