E2 ANTIBACTERIAL FOAMING SKIN CLEANSER- benzalkonium chloride soap

E2 Antibacterial Foaming Skin Cleanser by

Drug Labeling and Warnings

E2 Antibacterial Foaming Skin Cleanser by is a Otc medication manufactured, distributed, or labeled by Betco Corporation, Ltd., Betco corporation, Ltd., Betco Corportation, Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

E2 Antibacterial Foaming Skin Cleanser

​Active Ingredient

Benzalkonium Chloride 0.13%

E2 Antibacterial Foaming Skin Cleanser

Uses

• For handwashing to decrease the bacteria on the skin.
• Recommended for repeated use.

E2 Antibacterial Foaming Skin Cleanser

Warnings

• For external use only.
• When using this product avoid contact with eyes. In case of contact flush with water
• Discontinue use is irritation or redness develops.
• Stop use and ask a doctor If irritation persists for more than 72 hours, or if condition persists for more than 72 hours.
• KEEP OUT OF REACH OF CHILDREN.
• If swallowed, get medical help or contact Poison Control Center right away.

E2 Antibacterial Foaming Skin Cleanser

Directions

• ​Read the entire label before using this product.
• ​Dispense 2 pumps of product in hands and scrub thoroughly over all surfaces of both hands for 15 seconds. Rinse with clean water.

E2 Antibacterial Foaming Skin Cleanser

Inactive Ingredients

​Water, coco-glucoside, laurtrimonium chloride, cocamidopropylamine oxide, citric acid.

E2 Antibacterial Foaming Skin Cleanser

Purpose

Antimicrobial

E2 Antibacterial Foaming Skin Cleanser

KEEP OUT OF REACH OF CHILDREN

E2 Antibacterial Foaming Skin Cleanser

INGREDIENTS AND APPEARANCE

E2 ANTIBACTERIAL FOAMING SKIN CLEANSER 
benzalkonium chloride soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 65601-817
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
CAPRYLYL/CAPRYL OLIGOGLUCOSIDE (UNII: E00JL9G9K0)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
WATER (UNII: 059QF0KO0R)
LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC)
TETRASODIUM EDTA (UNII: MP1J8420LU)
ALCOHOL (UNII: 3K9958V90M)
SODIUM BENZOATE (UNII: OJ245FE5EU)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65601-817-04	3780 mL in 1 JUG; Type 0: Not a Combination Product	01/17/2014
2	NDC: 65601-817-29	1000 mL in 1 BAG; Type 0: Not a Combination Product	01/17/2014
3	NDC: 65601-817-03	750 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/17/2014	09/11/2020
4	NDC: 65601-817-55	208000 mL in 1 DRUM; Type 0: Not a Combination Product	01/17/2014

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	01/17/2014

Labeler - Betco Corporation, Ltd. (005050158)

Registrant - Betco corporation, Ltd. (005050158)

Establishment
Name	Address	ID/FEI	Business Operations
Betco Corporation, Ltd.		005050158	label(65601-817) , manufacture(65601-817)