E2 SANITIZING HAND- e2 sanitizing hand soap 
KUTOL PRODUCTS COMPANY

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.

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F017 LIQUID E2 SANITIZING HAND SOAP

Active Ingredient

Benzalkonium Chloride 0.13% w/w

Purpose

Antibacterial Agent

Uses

For handwashing to help reduce bacteria on the skin that could cause disease.

Warnings

For external use only. Avoid contact with eyes. If contact occurs, flush with water.

Stop use and ask a doctor if, in rare instances, redness or irritation develops and persists for more than 72 hours.

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

Directions

To decrease bacteria on skin, apply small amount, covering hands with product for 30 seconds. Add water, lather, rinse.

Inactive Ingredients

Water, Cocamidopropyl PG-Dimonium Chloride Phosphate, Cocamidopropyl Betaine, PEG-6 Cocamide, Hydroxyethyl Cellulose, Laurtrimonium Chloride, Iodopropynyl Butylcarbamate, Methylisothiazolinone.

Kutol Product Co.
Cincinnati, OH 45241
www.Kutol.com

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E2 SANITIZING HAND 
e2 sanitizing hand soap
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50865-017
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.003 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)  
PEG-6 COCAMIDE (UNII: YZ6NLA4O1E)  
HYDROXYETHYL CELLULOSE (280 MPA.S AT 2%) (UNII: 12VCE9HR9E)  
LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:50865-017-03209000 mL in 1 DRUM; Type 0: Not a Combination Product09/15/2015
2NDC:50865-017-074000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/15/2015
3NDC:50865-017-094000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/15/2015
4NDC:50865-017-65800 mL in 1 BAG; Type 0: Not a Combination Product09/15/2015
5NDC:50865-017-672000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/15/2015
6NDC:50865-017-411000 mL in 1 BAG; Type 0: Not a Combination Product09/15/2015
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A09/15/2015
Labeler - KUTOL PRODUCTS COMPANY (004236139)
Registrant - Kutol Products Company (004236139)
Establishment
NameAddressID/FEIBusiness Operations
Kutol Products Company, Inc.004236139manufacture(50865-017)

Revised: 8/2023
Document Id: 03a8c5b9-b040-8b10-e063-6294a90ac578
Set id: 70357eaf-8cd8-4c5e-b7a8-ae2fbba0ca2e
Version: 8
Effective Time: 20230824
 
KUTOL PRODUCTS COMPANY