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Hand Wash by Vi-Jon

Medically reviewed on August 15, 2017

Dosage form: liquid
Ingredients: BENZALKONIUM CHLORIDE 1.3mg in 1mL
Labeler: Vi-Jon
NDC Code: 11344-466

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.

Mountain Falls Antibacterial Foaming Hand Wash

Active ingredient

Benzalkonium chloride 0.13%

Purpose

Antibacterial

Use

for handwashing to decrease bacteria on the skin

Warnings

For external use only: hands only

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

Stop use and ask a doctor if
  • irritation or redness develops
  • 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
  • wet hands
  • apply palmful to hands
  • scrub thoroughly
  • rinse thoroughly

Inactive ingredients

water, glycerin, lauramine oxide, cocamidopropyl betaine, Aloe barbadensis leaf juice, PEG-150 distearate, cocamide MEA, fragrance, citric acid, tetrasodium EDTA, DMDM hydantoin, benzophenone-4 yellow 5, red 4

Rear Label Text

Manufactured by:  Vi-Jon, Inc., St. Louis, MO 63114

Questions or Comments?  1-888-593-0593

Made in the USA with US and foreign parts

Principal Display Panel

Mountain Falls antibacterial foaming hand wash

helps kill harmful germs

gentle and mild

32 FL OZ (1 QT) (946 mL)

HAND WASH 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11344-466
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 
GLYCERIN 
LAURAMINE OXIDE 
COCAMIDOPROPYL BETAINE 
ALOE VERA LEAF 
PEG-150 DISTEARATE 
COCO MONOETHANOLAMIDE 
CITRIC ACID MONOHYDRATE 
EDETATE SODIUM 
DMDM HYDANTOIN 
sulisobenzone 
FD&C YELLOW NO. 5 
FD&C RED NO. 4 
Packaging
#Item CodePackage Description
1NDC:11344-466-96221 mL in 1 BOTTLE, PLASTIC
2NDC:11344-466-44532 mL in 1 BOTTLE, PLASTIC
3NDC:11344-466-45946 mL in 1 BOTTLE, PLASTIC
4NDC:11344-466-031479 mL in 1 BOTTLE, PLASTIC
5NDC:11344-466-571182 mL in 1 BOTTLE, PLASTIC
6NDC:11344-466-083780 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A02/17/2016
Labeler - Vi-Jon (150931459)
Registrant - Vi-Jon (088520668)
Establishment
NameAddressID/FEIOperations
Vi-Jon088520668manufacture(11344-466)

 
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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