E2 HAND SANITIZER solution

E2 Hand Sanitizer by

Drug Labeling and Warnings

E2 Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by US Chemical Corporation, Kutol Products Company, Kutol Products. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DOSAGE & ADMINISTRATION

Directions Wet hands and apply about 5 mL to palm of hand. Vigorously rub the surfaces of the lathered fingers, finger tips, areas between the fingers, hands and arms. Wash hands thoroughly for 30 seconds. Rinse had thoroughly with potable water. Follow by thorough drying of cleaned hands and arms before handling food.

INACTIVE INGREDIENT

Inactive Ingredients Water, Cocamidoprpyl PG-Domonium Chloride Phosphate, Cocamidoprpyl Betaine, PEG-6 Cocamide, Hydroxyethylcellulose, Laurtrimonium Chloride, Iodopropynyl, Butylcarbamate, Methylisothiazolinone.

INDICATIONS & USAGE

Uses For hand washing to decrease bacteria on skin.

ACTIVE INGREDIENT

Active Ingredient Benzalkonium Chloride 0.13% w/w

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN

Kep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

PURPOSE

Purpose Antibacterial Agent

WARNINGS

Warnings For external use only. Avoid contact with eyes. In case of contact, flush with plenty of water. Stop use and ask a doctor if irritation persists.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

E2 HAND SANITIZER 
e2 hand sanitizer solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 61307-017
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.013 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
CETYL HYDROXYETHYLCELLULOSE (350000 MW) (UNII: T7SWE4S2TT)
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE (UNII: 205Z54J075)
PEG-6 COCAMIDE (UNII: YZ6NLA4O1E)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 61307-017-09	3785 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/10/2015
2	NDC: 61307-017-31	1500 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/10/2015

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	12/10/2015

Labeler - US Chemical Corporation (031457842)

Registrant - Kutol Products Company (004236139)

Establishment
Name	Address	ID/FEI	Business Operations
Kutol Products		004236139	manufacture(61307-017)