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Hand Wash by ULINE

Medically reviewed on March 28, 2018

Dosage form: soap
Ingredients: BENZALKONIUM CHLORIDE 1.3mg in 1mL
Labeler: ULINE
NDC Code: 69790-466

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.

Drug Facts

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

Adverse reactions

Distributed by Harmon Stores, Inc

650 Liberty Ave Union, NJ 07083 USA

Harmon Stores, Inc.

Visit us at www.facevalues.com

REFILL ONLY WITH FOAMING HAND SOAP, REGULAR LIQUID HAND SOAP WILL NOT FOAM.

package lable

ULINE

ANTIBACTERIAL

HAND SOAP

S-20662

7.5 FL OZ ( 221 mL)

HAND WASH 
benzalkonium chloride soap
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69790-466
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:69790-466-96221 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A02/17/2016
Labeler - ULINE (039612668)
Registrant - Vi-Jon (790752542)
Establishment
NameAddressID/FEIOperations
Vi-Jon088520668manufacture(69790-466)

 
ULINE

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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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