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Foaming Hand Sanitizer by Vi-Jon

Medically reviewed on December 5, 2017

Dosage form: liquid
Ingredients: BENZALKONIUM CHLORIDE 1.3mg in 1mL
Labeler: Vi-Jon
NDC Code: 0869-0492

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

Claims

For questions, please visit www.mycleanpath.com or call (213) 568-0006.  Manufactured by Vi-Jon, Inc. St. Louis MO 63114

To Dilute: Flip bottle, squeeze pod to fill measuring cup.  Remove pump, add distilled water to fill line.  Air bubble in cup is normal.  CleanPath Refill pod only to be used with CleanPath Reusable Bottle.  Do not use for any other purpose.

effctive at eliminating 99.9% of many common harmful germs in as little as 15 seconds

Active ingredient

Concentrate: Benzalkonium chloride 1.3%

Use Dilution: Benzalkonium chloride 0.13%

Purpose

Antiseptic

Use

for handwashing to decrease bacteria on the skin

Warnings

For external use only

When using this product
  • do not use in the eyes.  In case of contact with eyes, flush thoroughly with water
  • avoid contact with broken skin
  • dilute with distilled water before use because acidic or hard water may render the product inactive

Stop use and ask a doctor if

condition persists 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
  • follow dilution instructions
  • wet hands thoroughly with product and allow to dry without wiping

Inactive ingredients

water, DMDM hydantoin, fragrance, cetrimonium chloride, isoceteth-20, disodium cocamphodipropionate, PPG-2 hydroxyethyl coco/isostearamide, laureth-23, citric acid, blue 1, ext. violet 2, red 40

Adverse reaction

Manufactured by Vi-Jon, Inc.

St. Louis, MO 63114

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FOAMING HAND SANITIZER 

Refill Pod

concentrate makes 3 bottles

CleanPath

PREMIUM

FOAMING HAND SANITIZER

Natural spring

eleminated 99.9% of germs

REDUCE WATSE

Natural Spring

Remove Shrink Sleeve Before Recycling

3 FL OZ (90 mL)

FOAMING HAND SANITIZER 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0869-0492
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
water 
DMDM HYDANTOIN 
CETRIMONIUM CHLORIDE 
ISOCETETH-20 
DISODIUM COCOAMPHODIPROPIONATE 
PPG-2 HYDROXYETHYL COCO/ISOSTEARAMIDE 
LAURETH-23 
CITRIC ACID MONOHYDRATE 
FD&C BLUE NO. 1 
EXT. D&C VIOLET NO. 2 
FD&C RED NO. 40 
Packaging
#Item CodePackage Description
1NDC:0869-0492-2190 mL in 1 PACKAGE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A09/03/2014
Labeler - Vi-Jon (790752542)
Registrant - Vi-Jon (790752542)
Establishment
NameAddressID/FEIOperations
Vi-Jon790752542manufacture(0869-0492)

 
Vi-Jon

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Further information

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

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