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SCRUBS Foaming Hand Sanitizer (ITW Dymon)

Available Formats

Dosage Form Package Information Links
SOLUTION 252 mL in 1 BOTTLE, PUMP (51239-1929-7) Label Information

Complete SCRUBS Foaming Hand Sanitizer Information

  • ACTIVE INGREDIENT

    Active Ingredients                                                                                           Purpose

    n-alkyl dimethyl benzyl ammonium chloride (0.1%)....................................Antiseptic

    n-alkyl dimethyl ethyl benzyl ammonium chloride (0.1%)..........................Antiseptic


  • STOP USE

    Stop use and ask a doctor

    • if irritation arises and persists for more than 72 hours

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.  If swallowed, get medical help or contact a Poison Control Center right away.


  • WHEN USING

    When using this product

    • do not get into eyes.  If contact occurs rinse eyes thoroughly with water.

  • PURPOSE

    Uses

    • For hand washing to decrease bacteria on skin.
    • Recommended for repeated use.

  • WHEN USING

    Directions

    • Wet hands thoroughly with product and allow to dry without wiping.
    • Children under six years of age should be supervised when using this product.



  • WHEN USING

    Warnings
    Flammable, keep away from heat and flame.

    For external use only.

  • QUESTIONS

    Inactive Ingredients
    Water, ethanol, Mineral Oil, Isoproply Myristate, C12-C14 Sec-pareth-5
  • INGREDIENTS AND APPEARANCE
    SCRUBS FOAMING HAND SANITIZER  SCRUBS
    hand sanitizer foam solution
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:51239-1929
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP) BENZETHONIUM CHLORIDE 0.1 g  in 970 mL
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.1 g  in 970 mL
    Inactive Ingredients
    Ingredient Name Strength
    Mineral Oil (UNII: T5L8T28FGP) 0.7 g  in 970 mL
    Isopropyl Myristate (UNII: 0RE8K4LNJS) 0.3 g  in 970 mL
    Alcohol (UNII: 3K9958V90M) 20 g  in 970 mL
    Water (UNII: 059QF0KO0R) 78.02 g  in 970 mL
    Product Characteristics
    Color      Score     
    Shape Size
    Flavor LEMON Imprint Code
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:51239-1929-7 252 mL in 1 BOTTLE, PUMP
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333 10/01/2009
    Labeler - ITW Dymon (103307604)
    Registrant - ITW Dymon (103307604)
    Establishment
    Name Address ID/FEI Business Operations
    ITW Dymon 103307604 manufacture