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Alcohol Free Foaming Hand Sanitizer

Medically reviewed on September 12, 2016

Dosage form: soap
Ingredients: BENZALKONIUM CHLORIDE 1.3mg in 1mL
Labeler: Betco Corporation, Ltd.
NDC Code: 65601-700

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.

Alcohol Free Foaming Hand Sanitizer

Alcohol Free Foaming Hand Sanitizer

​Active Ingredient

Benzalkonium Chloride 0.13%

Alcohol Free Foaming Hand Sanitizer

Uses

  • Hand sanitizer to remove microorganisms on the skin.
  • Use this product when soap and water are not available.

Alcohol Free Foaming Hand Sanitizer

Warnings

  • For external use only.
  • Avoid contact with eyes. If contact occurs, rinse thoroughly with water.
  • Discontinue use is irritation or redness develops.
  • If irritation persists for more than 72 hours, consult a physician.
  • KEEP OUT OF REACH OF CHILDREN.
  • If swallowed, get medical help or contact a Poison Control Center right away.

Alcohol Free Foaming Hand Sanitizer

Directions

  • ​Read the entire label before using this product.
  • ​Dispense 2 pumps of product onto palm of hand and rub thoroughly over all surfaces of both hands until dry.

Alcohol Free Foaming Hand Sanitizer

Inactive Ingredients

Deionized ​Water, Sodium PCA, PEG/PPG-8/3 Laurate, Dimethicone,  PEG-3 Cocamide, Fragrance, Methyl Chloro Isothiazolinone, Methyl Isothiazolinone,  D&C Green #5.

Alcohol Free Foaming Hand Sanitizer

Questions or Comments?Phone: (800) 777-9343

MDS information:​(800) 891-4965

Alcohol Free Foaming Hand Sanitizer

Purpose

Antiseptic

Alcohol Free Foaming Hand Sanitizer

KEEP OUT OF REACH OF CHILDREN

Alcohol Free Foaming Hand Sanitizer

ALCOHOL FREE FOAMING HAND SANITIZER 
benzalkonium chloride soap
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65601-700
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 
SODIUM PYRROLIDONE CARBOXYLATE 
POLYETHYLENE GLYCOL 400 
DIMETHICONE 
PEG-3 COCAMINE 
MAGNESIUM CHLORIDE 
2-METHYL-4-ISOTHIAZOLIN-3-ONE HYDROCHLORIDE 
D&C GREEN NO. 5 
Product Characteristics
ColorblueScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage Description
1NDC:65601-700-5350 mL in 1 BOTTLE, PUMP
2NDC:65601-700-291000 mL in 1 BAG
3NDC:65601-700-043780 mL in 1 BOTTLE, PLASTIC
4NDC:65601-700-57550 mL in 1 BOTTLE, PUMP
5NDC:65601-700-55207900 mL in 1 DRUM
6NDC:65601-700-03750 mL in 1 BOTTLE, PUMP
7NDC:65601-700-051250 mL in 1 BOTTLE, PUMP
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A11/12/2012
Labeler - Betco Corporation, Ltd. (070307547)
Registrant - Betco corporation, Ltd. (070307547)
Establishment
NameAddressID/FEIOperations
Betco Corporation, Ltd.070307547manufacture(65601-700), pack(65601-700), label(65601-700)

 
Betco Corporation, Ltd.

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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