Label: CHEMSTAR INSTANTFOAM NONALCOHOL SANITIZER- benzalkonium chloride liquid 

  • Label RSS
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

NOTE: Most over the counter (OTC) are not reviewed and approved by the FDA. However, they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated 12/12

If you are a consumer or patient please visit this version.

  • Active ingredient

    Benzalkonium Chloride, 0.13%

    Close
  • Purpose

    Antibacterial

    Close
  • Uses

    For hand sanitizing to reduce bacteria on the skin

    Close
  • 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.

    Close
  • Directions

    Apply one shot to dry hands, rub into skin

    No rinsing required

    Close
  • Inactive ingredients

    Water, Propylene Glycol, Aloe Barbadensis Leaf Juice, Cocamidopropyl Betaine, Lauramine Oxide, Tetrasodium EDTA, Fragrance, Citric Acid, Magnesium Nitrate, Methylchloroisothiazolinone, Magnesium Chloride, Methylisothiazolinone, Blue 1 (CI 42090), Red 33 (CI 17200)

    Close
  • Chemstar Non-Alcohol Foaming Hand Sanitizer

    Chemstar

    product label

    Close
  • INGREDIENTS AND APPEARANCE
    CHEMSTAR INSTANTFOAM NONALCOHOL SANITIZER 
    benzalkonium chloride liquid
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:11084-111
    Route of Administration TOPICAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE 1.3 mg  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER  
    PROPYLENE GLYCOL  
    ALOE VERA LEAF  
    COCAMIDOPROPYL BETAINE  
    LAURAMINE OXIDE  
    EDETATE SODIUM  
    ANHYDROUS CITRIC ACID  
    D&C RED NO. 33  
    FD&C BLUE NO. 1  
    METHYLCHLOROISOTHIAZOLINONE  
    METHYLISOTHIAZOLINONE  
    MAGNESIUM NITRATE  
    MAGNESIUM CHLORIDE  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:11084-111-27 1000 mL in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333A 12/01/2012
    Labeler - Deb USA, Inc. (607378015)
    Registrant - Deb USA, Inc. (607378015)
    Establishment
    Name Address ID/FEI Business Operations
    Deb USA, Inc. 607378015 manufacture(11084-111)
    Close