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Disney Princess Antibacterial Hand Wipes

Medically reviewed on February 19, 2018

Dosage form: liquid
Ingredients: BENZALKONIUM CHLORIDE 1mg in 1mL
Labeler: Concept Products Ltd
NDC Code: 76183-001

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.

Disney Princess Antibacterial Hand Wipes

Disney Princess Antibacterial Hand Wipes


Active Ingredient

Benzalkonium Chloride 0.1%

Purpose

Antibacterial

Use

decreases bacteria on skin

Warnings

For external use only

Do not use if you are allergic to any of the ingredients.

When using this product avoid contact with eyes. If contact occurs, rinse thoroughly with water.

Stop use and ask a doctor if irritation or rash develops and continues for more than 72 hours.

Keep out of reach of children.If swallowed, get medical help or contact a Poison Control Center right away.

Directions
  • Lift package label to open and remove wipe.
  • Wipe hands thoroughly. Allow to dry.
  • Discard wipe in trash. Do not flush.
  • Re-seal package after each use to avoid evaporation.
  • For children under 2 year, consult a physician before use.

Inactive Ingredients

Water, Propylene Glycol, Phenoxyethanol, Cetearyl Isononanoate, Ceteareth-20, Cetearyl Alcohol, Glyceryl Stearate, Glycerin, Ceteareth-12, Cetyl Palmitate, Disodium EDTA, Tocopheryl Acetate, Aloe Barbadensis Leaf Extract,2-Bromo-2-Nitropropane-1,3-Diol, Citric Acid, Methylchloroisothiazolinone, Methylisothiazolinone


Questions?

Call Toll Free 1-800-635-3969

Distributed by:

Peachtree Playthings

P.O.Box 723665, Atlanta, GA 31139

MADE IN CHINA (TIANJIN)

Disney

www.disneyprincess.com

2013 Peachtree Playthings

All Rights Reserved

www.peachtreeplaythings.com






Product labeling

DISNEY PRINCESS ANTIBACTERIAL HAND WIPES  
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76183-001
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE1 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
PROPYLENE GLYCOL 
PHENOXYETHANOL 
POLYOXYL 20 CETOSTEARYL ETHER 
CETOSTEARYL ALCOHOL 
GLYCERYL MONOSTEARATE 
GLYCERIN 
CETEARETH-12 
CETYL PALMITATE 
EDETATE DISODIUM 
.ALPHA.-TOCOPHEROL ACETATE 
ALOE VERA LEAF 
BRONOPOL 
CITRIC ACID MONOHYDRATE 
METHYLCHLOROISOTHIAZOLINONE 
METHYLISOTHIAZOLINONE 
Packaging
#Item CodePackage Description
1NDC:76183-001-0141.45 mL in 1 POUCH
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E05/02/2012
Labeler - Concept Products Ltd (421342352)
Establishment
NameAddressID/FEIOperations
Concept Products Ltd421342352manufacture(76183-001)

 
Concept Products Ltd

Further information

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

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