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ICI Non-Alcohol Hand Sanitizer Dye and Fragrance Free

Medically reviewed on September 4, 2017.

Dosage form: liquid
Ingredients: BENZALKONIUM CHLORIDE 0.0013g in 1mL
Labeler: Deb USA, Inc.
NDC Code: 11084-155

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.

Drug Facts

Active ingredient

BENZALKONIUM CHLORIDE, 0.13%

Purpose

Antibacterial

Uses

for hand sanitizing to reduce bacteria on the skin

Warnings

For external use only

When using this product

avoid contact with eyes. In case of eye contact, flush with water.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

apply foaming sanitizer to cover hands

rub into skin

no rinsing required

Inactive ingredients

ALOE BARBADENSIS LEAF JUICE, AQUA (WATER), COCAMIDOPROPYL BETAINE, LAURAMINE OXIDE, MAGNESIUM CHLORIDE, MAGNESIUM NITRATE, METHYLCHLOROISOTHIAZOLINONE, METHYLISOTHIAZOLINONE, PROPYLENE GLYCOL, TETRASODIUM EDTA

ICI

Non-Alcohol Hand Sanitizer

Antiseptico para manos en espuma - sin alcohol

Distributed in the USA by:

Illinois Correctional Industries

Springfield, IL 62794

1-800-634-0213

Made in USA

Stock #

ICIAFS120TF/0815

1.2 L

(40.6 fl oz)

ICI NON-ALCOHOL HAND SANITIZER DYE AND FRAGRANCE FREE 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11084-155
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE0.0013 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF 
WATER 
COCAMIDOPROPYL BETAINE 
LAURAMINE OXIDE 
MAGNESIUM CHLORIDE 
MAGNESIUM NITRATE 
METHYLCHLOROISOTHIAZOLINONE 
METHYLISOTHIAZOLINONE 
PROPYLENE GLYCOL 
EDETATE SODIUM 
Packaging
#Item CodePackage Description
1NDC:11084-155-121200 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A08/27/2015
Labeler - Deb USA, Inc. (607378015)
Establishment
NameAddressID/FEIOperations
Deb USA, Inc.078805627manufacture(11084-155)

 
Deb USA, Inc.

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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