HAND SANITIZING GEL- instant hand sanitizing gel gel

Hand Sanitizing Gel by

Drug Labeling and Warnings

Hand Sanitizing Gel by is a Otc medication manufactured, distributed, or labeled by US Chemical Corporation, Kutol Products Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DOSAGE & ADMINISTRATION

Directions Place enough product in your palm to thoroughly cover your hands. Rub hands together briskly until dry. Children under 6 years of age should be supervised when using this product.

INACTIVE INGREDIENT

Inactive Ingredients Water, Glycerin, Propylene Glycol, Isopropyl Myristate, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, Carbomer, Aminomethyl Propanol.

INDICATIONS & USAGE

Uses Hand sanitizer to help reduce bacteria on the skin that could cause disease, Recommended for repeated use.

ACTIVE INGREDIENT

Active Ingredient Ethyl Alcohol 62% v/v

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.

PURPOSE

Purpose Antibacterial Agent

WARNINGS

Warnings Flammable. Keep away from fire or flame. For external use only. Avoid contact with eyes. In case of contact, flush with plenty of water. Stop and ask a doctor if irritation or rash appears and persists.

PRINCIPAL DISPLAY PANEL

Principal Dispaly

INGREDIENTS AND APPEARANCE

HAND SANITIZING GEL 
instant hand sanitizing gel gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 61307-056
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CARBOMER 1342 (UNII: 809Y72KV36)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL 1,2-DISTEARATE (UNII: T65PN3O37H)
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
AMINOMETHYL PROPANEDIOL (UNII: CZ7BU4QZJZ)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 61307-056-31	1500 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/07/2013

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/07/2013

Labeler - US Chemical Corporation (031457842)

Registrant - Kutol Products Company (004236139)

Establishment
Name	Address	ID/FEI	Business Operations
Kutol Products Company		004236139	manufacture(61307-056)