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Appeal Non-Alcohol Foaming Hand Sanitizer

Dosage form: liquid
Ingredients: BENZALKONIUM CHLORIDE 0.13mL in 100mL
Labeler: Deb USA, Inc.
NDC Code: 11084-106

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

Acitive 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 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 one shot to dry hands, rub into skin

No rinsing required

Inactive ingredients

Water, Propylene Glycol, Aloe Barbadensis Leaf Juice, Cocamidopropyl Betaine, Lauramine Oxide, Tetrasodium EDTA, Magnesium Nitrate, Methylchloroisothiazolinone, Magnesium Chloride, Methylisothiazolinone

APP17103

appeal

Non-alcohol Foaming Hand Sanitizer

1 Liter

33.8 Fluid Ounces

Made in the USA by Deb

deb foam technology

Distributed exclusively by:

AmSan

America's Leading Supplier of Janitorial and Cleaning Products

APPEAL NON-ALCOHOL FOAMING HAND SANITIZER 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11084-106
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE0.13 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
PROPYLENE GLYCOL 
ALOE VERA LEAF 
COCAMIDOPROPYL BETAINE 
LAURAMINE OXIDE 
EDETATE SODIUM 
MAGNESIUM NITRATE 
METHYLCHLOROISOTHIAZOLINONE 
MAGNESIUM CHLORIDE 
METHYLISOTHIAZOLINONE 
Packaging
#Item CodePackage Description
1NDC:11084-106-271000 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: 09/2010
 
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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