Antibacterial Hand Soap

Antibacterial Hand Soap

Drug Labeling and Warnings

Drug Details

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ANTIBACTERIAL HAND WASH- benzalkonium chloride soap 
Vi-Jon, Inc.

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.

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Antibacterial Hand Soap

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, cocamidopropyl betaine, lauramine oxide, PEG-150 distearate, sodium chloride, cetrimonium chloride, decyl glucoside, glycerin, fragrance, disteareth-75 IPDI, citric acid, tetrasodium EDTA, DMDM hydantoin, benzophenone-4, blue 1, red 33

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

helps kill harmful germs

for softer, smoother feeling hands

Antibacterial liquid hand soap

Spring rain

11.25 FL OZ (332 mL)

image description

942.000/942AA

ANTIBACTERIAL HAND WASH 
benzalkonium chloride soap
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 11344-942
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)  
GLYCERIN (UNII: PDC6A3C0OX)  
DISTEARETH-75 ISOPHORONE DIISOCYANATE (UNII: 5365FJ30SC)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
EDETATE SODIUM (UNII: MP1J8420LU)  
DMDM HYDANTOIN (UNII: BYR0546TOW)  
BENZOPHENONE (UNII: 701M4TTV9O)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 11344-942-81332 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product11/01/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A11/01/2017
Labeler - Vi-Jon, Inc. (150931459)
Registrant - Vi-Jon, Inc. (790752542)
Establishment
NameAddressID/FEIBusiness Operations
Vi-Jon, Inc.088520668manufacture(11344-942)

Revised: 12/2018
 
Vi-Jon, Inc.


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