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Sani-Kleen (Eco-Logics, Inc.)

Available Formats

Dosage Form Package Information Links
GEL 3.78 L in 1 JUG (30056-002-28) Label Information
GEL .006 L in 1 POUCH (30056-002-06) Label Information
GEL .03 L in 1 BOTTLE (30056-002-01) Label Information

Complete Sani-Kleen Information

  • ACTIVE INGREDIENT

    Active Ingredient                                   Purpose

    Ethyl Alcohol 62%..............................................Antibacterial



  • Use

    Use for hand sanitizing to decrease bacteria on the skin.


  • Warnings

    Warnings

    For external use only. Flammable. Keep away from heat and flame.

    Do not store above 105 F. May discolor some fabrics.


  • When using this product

    When using this product

    avoid contact with eyes. In case of eye contact, flush with water.


  • Stop use and ask a doctor if

    Stop use and ask a doctor if

    irritation or redness develops, or if condition persists for more than 72 hours.


  • Keep out of the reach of children.

    Keep out of the reach of children.

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


  • Directions

    Directions

    • Apply a small amount onto palm of hand
    • Rub thoroughly over all surfaces of both hands
    • Rub hands together briskly until dry

    Purpose

    Active Ingredients                                                    Purpose

    Ethyl Alcohol 62%....................................................Antibacterial

    Directions

    Directions

    • Apply a small amount onto palm of hand
    • Rub thoroughly over all surfaces of both hands
    • Rub hands together briskly until dry

  • Inactive Ingredients

    Inactive Ingredients

    Water, Aloe Barbadensis, Tocopheryl, Matricaria Chamomilla, Glycerin, Propylene Glycol, Isopropyl Myristate, Aminoethyl Propanol,

    Carbomer, Parfum (if scented).


  • INGREDIENTS AND APPEARANCE
    SANI-KLEEN  INSTANT HAND SANITIZER
    ethyl alcohol gel
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:30056-002
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M) Alcohol 620 mL  in 1 L
    Inactive Ingredients
    Ingredient Name Strength
    Water (UNII: 059QF0KO0R)  
    Aloe Vera Leaf (UNII: ZY81Z83H0X)  
    Alpha-Tocopherol (UNII: H4N855PNZ1)  
    Chamomile (UNII: FGL3685T2X)  
    Glycerin (UNII: PDC6A3C0OX)  
    Propylene Glycol (UNII: 6DC9Q167V3)  
    Isopropyl Myristate (UNII: 0RE8K4LNJS)  
    Aminomethylpropanol (UNII: LU49E6626Q)  
    Carbomer Homopolymer Type C (UNII: 4Q93RCW27E)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:30056-002-01 .03 L in 1 BOTTLE
    2 NDC:30056-002-06 .006 L in 1 POUCH
    3 NDC:30056-002-28 3.78 L in 1 JUG
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333A 11/01/2009
    Labeler - Eco-Logics, Inc. (047667022)