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PURELL Hand Sanitizing Wipes Clean Refreshing Scent

Medically reviewed on October 14, 2016

Dosage form: liquid
Ingredients: BENZALKONIUM CHLORIDE 0.000131
Labeler: GOJO Industries, Inc.
NDC Code: 21749-359

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.

PURELL Hand Sanitizing Wipes Clean Refreshing Scent

Active ingredient

Benzalkonium Chloride 0.13%

Active ingredient

Benzalkonium Chloride 0.13%

Purpose

Antimicrobial

Use

Hand sanitizer to help reduce bacteria on the skin

Warnings

For external use only

When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash appears and lasts

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

Directions

• Wet hands thoroughly with product and allow to dry

• Children under 6 years of age should be supervised when using PURELL


Inactive ingredients

Water (Aqua), Decyl Glucoside, Glycerin, Fragrance(Parfum), Methylparaben, Phenoxyethanol, Propylparaben

PURELL HAND SANITIZING WIPES CLEAN REFRESHING SCENT 
benzalkonium chloride wipe liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:21749-359
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE0.00013 
Inactive Ingredients
Ingredient NameStrength
WATER 
DECYL GLUCOSIDE 
GLYCERIN 
METHYLPARABEN 
PHENOXYETHANOL 
PROPYLPARABEN 
Packaging
#Item CodePackage Description
1NDC:21749-359-1515 LIQUID in 1 PACKAGE
2NDC:21749-359-2020 LIQUID in 1 PACKAGE
3NDC:21749-359-4040 LIQUID in 1 PACKAGE
4NDC:21749-359-7070 LIQUID in 1 PACKAGE
5NDC:21749-359-1010 LIQUID in 1 PACKAGE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E08/01/2014
Labeler - GOJO Industries, Inc. (004162038)

 
GOJO Industries, Inc.

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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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