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Antibacterial Hand Wash by Vi-Jon, Inc

Medically reviewed on Mar 28, 2018

Dosage form: liquid
Ingredients: BENZALKONIUM CHLORIDE 1.313mg in 1mL
Labeler: Vi-Jon, Inc
NDC Code: 11344-416

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

Active ingredient section

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 the eyes.  If contact occurs, rinse eyes 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, PEG-150 distearate, Punica granatum fruit extract (pomegranate), Rubus idaeus (raspberry) fruit extract, Vaccinium macrocarpon (cranberry) fruit extract, tocopheryl acetate, Camellia oleifera leaf extract (green tea), cocamide MEA, fragrance, citric acid, tetrasodium EDTA, DMDM hydantoin, benzophenone-4, red 33, orange 4

Adverse Reactions

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

416.001/416AB

Principal Display Panel

mountain

falls

helps

kill harmful

germs

gentle

on skin

antibacterial

foaming

hand soap

energy berry

7.5 FL OZ (221 mL)

ANTIBACTERIAL HAND WASH 
benzalkonium chloride 0.13% liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11344-416
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE1.313 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
water 
GLYCERIN 
LAURAMINE OXIDE 
COCAMIDOPROPYL BETAINE 
PEG-150 DISTEARATE 
POMEGRANATE 
RASPBERRY 
CRANBERRY 
.ALPHA.-TOCOPHEROL ACETATE 
GREEN TEA LEAF 
COCO MONOETHANOLAMIDE 
CITRIC ACID MONOHYDRATE 
EDETATE SODIUM 
DMDM HYDANTOIN 
SULISOBENZONE 
D&C RED NO. 33 
D&C ORANGE NO. 4 
Packaging
#Item CodePackage Description
1NDC:11344-416-96221 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A03/27/2017
Labeler - Vi-Jon, Inc (150931459)
Registrant - Vi-Jon, Inc (790752542)
Establishment
NameAddressID/FEIOperations
Vi-Jon. nc150931459manufacture(11344-416)

 
Vi-Jon, Inc

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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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