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

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Foaming Antiseptic Hand Cleaner

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

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.

Handwash to help decrease bacteria on the skin.

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.

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

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. If swallowed, get medical help or contact a poison control center right away.

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HUSKY 575 FOAMING ANTISEPTIC HAND CLEANER 
foaming antiseptic hand cleaner solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63779-340
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN20.8 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63779-340-771100 mL in 1 BOTTLE, PLASTIC
2NDC:63779-340-093785 mL in 1 BOTTLE, PLASTIC
3NDC:63779-340-1750 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A07/08/2013
Labeler - Canberra Corporation (068080621)
Establishment
NameAddressID/FEIBusiness Operations
Kutol Products Company, Inc.004236139manufacture(63779-340) , analysis(63779-340) , pack(63779-340)

Revised: 1/2014
Document Id: dbbb387f-137a-43a6-a24e-5458b382b5e3
Set id: 959d1525-2681-4912-9711-fa2c4a5b152d
Version: 1
Effective Time: 20140103
 
Canberra Corporation