Label: ALCOSCRUB HAND CLEANER- alcohol liquid

  • NDC Code(s): 55863-700-04, 55863-700-16, 55863-700-27, 55863-700-32
  • Packager: Erie Scientific, LLC.
  • 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 03/13

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

  • ACTIVE INGREDIENT

    Ethyl Alcohol 62 % v/v

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  • PURPOSE

    For handwashing  to decrease bacteria on skin.

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  • Keep Out of Reach of Children

    If swallowed, contact a physician or poison center

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  • Indications & Usage Section

    For hand cleaning to decrease bacteria on skin

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  • WARNINGS


    Flammable. Keep away from heat of flames. For external use only. Do not use in the eyes.

    Discontinue use if redness and irritation develop.  If condition persists for more than 72 hours, consult a physician.  If swallowed, contact a physician or poison control center.  Keep out of the reach of children.

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  • Dosage & Administration Section

    Apply a small amount to palm.  Briskly rub, covering hands with product until dry.

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  • Inactive ingredients

    Water, Glycerin, Carbomer, Propylene glycol, Isopropyl Myristate, Triethanolamine, Aloe Barbadensis Leaf, Tocopheryl acetate

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  • INGREDIENTS AND APPEARANCE
    ALCOSCRUB  HAND CLEANER
    alcohol liquid
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:55863-700
    Route of Administration TOPICAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ALCOHOL (ALCOHOL) ALCOHOL 1 mL  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    Water  
    Glycerin  
    Propylene Glycol  
    Isopropyl Myristate  
    Aloe Vera Flower  
    .ALPHA.-TOCOPHEROL ACETATE, DL-  
    Trolamine  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:55863-700-04 118 mL in 1 BOTTLE
    2 NDC:55863-700-16 472 mL in 1 BOTTLE
    3 NDC:55863-700-27 800 mL in 1 POUCH
    4 NDC:55863-700-32 944 mL in 1 BOTTLE, PUMP
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333E 01/03/2009
    Labeler - Erie Scientific, LLC. (361605223)
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