Veti-Foam

Dosage form: liquid
Ingredients: BENZETHONIUM CHLORIDE 2.0g in 1.0L
Labeler: MWI/Vet One
NDC Code: 13985-529

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.

Veti-Foam Hand Soap

Active ingredient(s)

 Benzethonium Chloride 0.20%

Purpose

Use(s)

 for hand washing to decrease bacteria on skin

Warnings

For external use only

Do not use

Ask a doctor before use if

Ask a doctor or pharmacist before use if

When using this product
  •  Avoid contact with eyes; in case of contact, thoroughly rinse eyes with water.  Seek medical attention if irritation persists.

Stop use and ask a doctor if
  • skin rash or redness develops when using this product 

Pregnancy/Breastfeeding

Keep out of reach of children

 If swallowed, get medical help or contact a Poison Control Center right away.

Directions

 Use 1-2 pumps of product on plam.  Rub lather completely around hands and between fingers.  Scrub thoroughly and rinse with water.

Other information

Storage

Inactive ingredients

 Aloe barbadensis (Aloe Vera) Leaf Juice, Ammonium lauryl Sulfate, Cocamidoprpyl Betaine, DMDM Hydantoin, FD&C Blue #1, Fragrance, Glycerin, Purified Water, EDTA

Questions

Principal Display Panel

16oz label

VETI-FOAM 
benzethonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:13985-529
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZETHONIUM CHLORIDE (BENZETHONIUM) BENZETHONIUM CHLORIDE2.0 g  in 1.0 L
Inactive Ingredients
Ingredient NameStrength
EDETATE SODIUM 
GLYCERIN 
WATER 
AMMONIUM LAURYL SULFATE 
COCAMIDOPROPYL BETAINE 
ALOE VERA LEAF 
DMDM HYDANTOIN 
FD&C BLUE NO. 1 
Product Characteristics
ColorBLUEScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage Description
1NDC:13985-529-160.473 L in 1 BOTTLE, PUMP
2NDC:13985-529-013.785 L in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart333A07/26/2010
Labeler - MWI/Vet One (019926120)
Registrant - Continental Manufacturing Chemist, Inc. (005278007)

Revised: 12/2011
 
MWI/Vet One

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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