Label: ELGIN INSTANT HAND SANITIZER- ethyl alcohol gel

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

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 Label Information

Updated June 28, 2010

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  • 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 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
  • Inactive Ingredients

    Inactive Ingredients

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

    Carbomer, Parfum (if scented).

  • PRINCIPAL DISPLAY PANEL

    image of gallon label

  • INGREDIENTS AND APPEARANCE
    ELGIN INSTANT HAND SANITIZER 
    ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:30056-005
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M) Alcohol620 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    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 CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:30056-005-283780 g in 1 JUG
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34706/01/2010
    Labeler - Eco-Logics, Inc. (047667022)
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