Medication Guide App

Aero IQ Antibacterial Quat

Dosage form: liquid
Ingredients: BENZALKONIUM CHLORIDE 1.30mL in 100mL
Labeler: Deb USA, Inc.
NDC Code: 11084-070

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, 1.30%

Purpose

Antibacterial

Uses

For hand washing to decrease bacteria on 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

Wet skin, rub soap onto hands

Wash for 15-20 seconds

Rinse and dry thoroughly

Inactive ingredients

Water, Cocamidopropyl Betaine, Undeceth-7, Cocamidopropylamine Oxide, Cocamide DEA, Lauramine Oxide, Tetrasodium EDTA, Citric Acid, Magnesium Nitrate, Methylchloroisothiazolinone, Magnesium Chloride, Methylisothiazolinone.

Aero IQ

Antibacterial Quat Foaming Soap

Food Handling Industry

Offers rapid kill rate against most common bacteria, yet remains mild to the skin.

NSF

deb foam technology

Proudly made in the USA by Deb

27280-01-112

2 Liter
 
67.6 fluid ounces



AERO IQ ANTIBACTERIAL QUAT  
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11084-070
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE1.30 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
COCAMIDOPROPYL BETAINE 
COCO DIETHANOLAMIDE 
LAURAMINE OXIDE 
EDETATE SODIUM 
CITRIC ACID MONOHYDRATE 
MAGNESIUM NITRATE 
METHYLCHLOROISOTHIAZOLINONE 
MAGNESIUM CHLORIDE 
METHYLISOTHIAZOLINONE 
Packaging
#Item CodePackage Description
1NDC:11084-070-202000 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A01/01/2010
Labeler - Deb USA, Inc. (607378015)
Establishment
NameAddressID/FEIOperations
Deb USA, Inc.607378015manufacture

Revised: 02/2011
 
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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