PureBac Foam Wash

Dosage form: liquid
Ingredients: CHLOROXYLENOL 0.5mL in 100mL
Labeler: Deb USA, Inc.
NDC Code: 11084-131

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

Chloroxylenol, 0.5%

Purpose

Antibacterial

Uses

For handwashing to reduce bacteria on the skin

Warnings

For external use only

When using this product avoid contact with eyes.

In case of eye contact, flush with water.

Keep out of reach of children.

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

Directions

Apply foaming cleanser to dry hands

Rub hands together to spead lather

Wash for 15-20 seconds

Rinse and dry hands thoroughly

Inactive ingredients

Water, Propylene Glycol, TEA-Lauryl Sulfate, PPG-24-Glycereth-24, Sodium Laureth Sulfate, Aloe Barbadensis Leaf Juice, Cocamidopropyl Betaine, Allantoin, Fragrance, Tetrasodium EDTA, Diazolidinyl Urea, Citric Acid, Methylparaben, Magnesium Nitrate, Propylparaben, Methylchloroisothiazolinone, Magnesium Chloride, Methylisothiazolinone.

deb

PureBac Foam Wash

MADE IN USA

1L

PUREBAC FOAM WASH 
chloroxylenol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11084-131
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CHLOROXYLENOL (PHENOL) CHLOROXYLENOL0.5 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
PROPYLENE GLYCOL 
TROLAMINE LAURYL SULFATE 
SODIUM LAURETH SULFATE 
ALOE VERA LEAF 
COCAMIDOPROPYL BETAINE 
ALLANTOIN 
EDETATE SODIUM 
DIAZOLIDINYL UREA 
CITRIC ACID MONOHYDRATE 
METHYLPARABEN 
MAGNESIUM NITRATE 
PROPYLPARABEN 
METHYLCHLOROISOTHIAZOLINONE 
MAGNESIUM CHLORIDE 
METHYLISOTHIAZOLINONE 
Packaging
#Item CodePackage Description
1NDC:11084-131-202000 mL in 1 BOTTLE, PLASTIC
2NDC:11084-131-271000 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E01/01/2010
Labeler - Deb USA, Inc. (607378015)
Establishment
NameAddressID/FEIOperations
Deb USA, Inc.607378015manufacture

Revised: 09/2010
 
Deb USA, Inc.

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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