HUSKY INSTANT HAND SANITIZER- husky instant hand sanitizer 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.

----------

Husky Instant Hand Sanitizer

For external use only.

Flammable. Keep away from heat or flame.

Do not use in the eyes. In case of 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, contact a physician or poison center.

Ethyl Alcohol 62% v/v.........Antibacterial Agent

Keep out of reach of children. If swallowed, contact a physician or poison center. 

Water, Glycerin, Propylene Glycol, Isopropyl Mryistate, Aloe Barbadensis Leaf, Carbomer, Tocopheryl Acetate (Vitamin E), Aminomethyl Propanol

63779-056-77 & 63779-056-27:

To decrease bacteria on skin, apply a small amount to palm. Briskly rub, covering hands with product until dry.

Children under 6 years of age should be supervised when using this product.

63779-056-87 & 63779-056-19:

To decrease bacteria on skin, apply a small amount to palm. Briskly rub, covering hands with product until dry.

63779-056-77 & 63779-056-27: For hand cleaning to decrease bacteria on skin that could cause disease. Recommended for repeated use.

63779-056-87: For handwashing to decrease bacteria on skin.

63779-056-19: For hand cleaning to decrease bacteria on skin.

For hand cleaning to decrease bacteria on skin that could cause disease. Recommended for repeated use.

Do not use in the eyes. In case of 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, contact a physician or poison center.

63779-056-19.jpg63779-056-19.jpg

63779-056-27.jpg63779-056-27.jpg

63779-056-77.jpg63779-056-77.jpg

63779-056-87.jpg63779-056-87.jpg

HUSKY INSTANT HAND SANITIZER 
husky instant hand sanitizer solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63779-056
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
POLYACRYLIC ACID (250000 MW) (UNII: 9G2MAD7J6W)  
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
.ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63779-056-19237 mL in 1 BOTTLE
2NDC:63779-056-8729 mL in 1 BOTTLE
3NDC:63779-056-27800 mL in 1 BAG
4NDC:63779-056-771100 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A05/22/2013
Labeler - Canberra Corporation (068080621)
Registrant - Kutol Products Company, Inc. (004236139)
Establishment
NameAddressID/FEIBusiness Operations
Kutol Products Company, Inc.004236139manufacture(63779-056) , analysis(63779-056) , pack(63779-056)

Revised: 2/2014
Document Id: 75d49f4b-545e-43a0-a4ab-eea93723178e
Set id: 0b0b6f36-3922-4e70-8d2f-9f2bbe88391a
Version: 1
Effective Time: 20140221
 
Canberra Corporation