HUSKY 575 FOAMING ANTISEPTIC HAND CLEANER- foaming antiseptic hand cleaner solution

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, Kutol Products Company, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Triclosan 0.5% w/w.......Antibacterial Handwashing

INACTIVE INGREDIENT

Water, Ammonium Lauryl Sulfate, Sodium Laureth Sulfate, Disodium Cocamido MIPA-Sulfosuccinate, Glycerin, Polyquaternium-7, Fragrance, Citric Acid, Polyquaternium-10, Aloe Barbadensis Leaf, Tocopheryl Acetate, Tetrasodium EDTA, DMDM Hydantoin, Green #3.

PURPOSE

Handwash to help decrease bacteria on the skin.

WARNINGS

For external use only.

Do not use in the eyes. In case of eye contact, immediately flush with water.

Stop use and ask a doctor if irritation or rash appears and lasts.

Keep out of reach of children. If swallowed, get medical help or contact a poison control center right away.

DOSAGE & ADMINISTRATION

To decrease bacteria on skin, apply a small amount, covering hands with product for 30 seconds. Add water, lather, rinse.

INDICATIONS & USAGE

Handwash to help decrease bacteria on the skin.

Do not use in the eyes. In case of eye contact, immediately flush with water.

Stop use and ask a doctor if irritation or rash appears and lasts.

Keep out of reach of children. If swallowed, get medical help or contact a poison control center right away.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a poison control center right away.

PRINCIPAL DISPLAY PANEL

63779-340-09.jpg

PRINCIPAL DISPLAY PANEL

63779-340-77.jpg

PRINCIPAL DISPLAY PANEL

    63779-340-17.jpg

INGREDIENTS AND APPEARANCE

HUSKY 575 FOAMING ANTISEPTIC HAND CLEANER 
foaming antiseptic hand cleaner solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63779-340
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X)	TRICLOSAN	20.8 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
POLYQUATERNIUM-10 (1000 MPA.S AT 2%) (UNII: GMR4PEN8PK)
EDETATE SODIUM (UNII: MP1J8420LU)
AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
GLYCERIN (UNII: PDC6A3C0OX)
POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600 KD) (UNII: 0L414VCS5Y)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)
DMDM HYDANTOIN (UNII: BYR0546TOW)
ISOSTEARAMIDOPROPYL MORPHOLINE LACTATE (UNII: 082Y3WQI5K)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63779-340-77	1100 mL in 1 BOTTLE, PLASTIC
2	NDC: 63779-340-09	3785 mL in 1 BOTTLE, PLASTIC
3	NDC: 63779-340-17	50 mL in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/08/2013

Labeler - Canberra Corporation (068080621)

Establishment
Name	Address	ID/FEI	Business Operations
Kutol Products Company, Inc.		004236139	manufacture(63779-340) , analysis(63779-340) , pack(63779-340)