CLEAN XPRESS ALCOHOL GEL INSTANT SKIN SANITIZER- clean xpress alcohol gel instant skin santizer liquid

Clean Xpress Alcohol Gel Instant Skin Sanitizer by

Drug Labeling and Warnings

Clean Xpress Alcohol Gel Instant Skin Sanitizer by is a Otc medication manufactured, distributed, or labeled by Spartan Chemical Company, Inc., Kutol Products Company, Inc, Kutol Products Company, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Ethyl Alcohol 62% v/v

INACTIVE INGREDIENT

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

DOSAGE & ADMINISTRATION

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.

PURPOSE

Hand sanitizer to help decrease bacteria on the skin that can cause disease.

Use between regular handwashings.

Recommended for repeated usage.

INDICATIONS & USAGE

Hand sanitizer to help decrease bacteria on the skin that can cause disease.

Use between regular hand washings.

Recommended for repeated usage.

Stop use and ask a doctor if irritation or rash appears and lasts. If swallowed get medical help or contact a Posion Control Center right away. Keep out of reach of children.

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.

WARNINGS

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 get medical help or contact a Posion Control Center right away.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CLEAN XPRESS ALCOHOL GEL INSTANT SKIN SANITIZER 
clean xpress alcohol gel instant skin santizer liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 64009-056
Route of Administration	Topical

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	65.2 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
POLYACRYLIC ACID (250000 MW) (UNII: 9G2MAD7J6W)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 64009-056-34	1000 mL in 1 BAG

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/22/2013

Labeler - Spartan Chemical Company, Inc. (005036728)

Registrant - Kutol Products Company, Inc (004236139)

Establishment
Name	Address	ID/FEI	Business Operations
Kutol Products Company, Inc.		004236139	manufacture(64009-056) , analysis(64009-056) , pack(64009-056)