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E2 SANITIZING HAND

Medically reviewed on February 14, 2018

Dosage form: soap
Ingredients: BENZALKONIUM CHLORIDE 0.003mg in 1mL
Labeler: KUTOL PRODUCTS COMPANY
NDC Code: 50865-017

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.

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

1703 label

1707 label

1709 label

1765 label

1767 label

E2 SANITIZING HAND 
e2 sanitizing hand soap
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50865-017
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE0.003 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
COCAMIDOPROPYL BETAINE 
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE 
PEG-6 COCAMIDE 
HYDROXYETHYL CELLULOSE (280 MPA.S AT 2%) 
LAURTRIMONIUM CHLORIDE 
METHYLISOTHIAZOLINONE 
IODOPROPYNYL BUTYLCARBAMATE 
Packaging
#Item CodePackage Description
1NDC:50865-017-03209000 mL in 1 DRUM
2NDC:50865-017-074000 mL in 1 BOTTLE, PLASTIC
3NDC:50865-017-094000 mL in 1 BOTTLE, PLASTIC
4NDC:50865-017-65800 mL in 1 BAG
5NDC:50865-017-672000 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A09/15/2015
Labeler - KUTOL PRODUCTS COMPANY (004236139)
Establishment
NameAddressID/FEIOperations
Kutol Products Company, Inc.004236139manufacture(50865-017), analysis(50865-017), label(50865-017), pack(50865-017)

 
KUTOL PRODUCTS COMPANY

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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