Label: ELEMENT CONTROL RINSE FREE HAND SANITIZER SOOTHING- 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 August 12, 2020

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  • Drug Facts

  • Active ingredient

    Ethyl Alcohol 70%

    Purpose

    Antiseptic

  • Use

    • helps reduce bacteria that potentially can cause disease.
    • helps prevent cross contamination by hand contact.
    • recommended for repeated use.
  • Warnings

    For external use only.

    Flammable. Keep away from heat or flame.

    Do not use 

    • in children less than 2 months of age or on open skin wounds.

    When using this product

    • keep out of eyes and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

    Stop use and ask a doctor

    • if irritation and redness develop

    Keep out of reach of children.

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

  • Directions

    • Place enough product on hands to cover all surfaces.
    • Rub hands together until dry.
    • Supervise children under 6 years of age when using this product to avoid swallowing.
  • Other information

    • avoid freezing and excessive heat above 40°C (104°F)
    • may discolor certain fabrics.
  • Inactive ingredients

    Water, Glycerin, Aloe Barbadensis Extract, Aminomethyl Propanol, Propylene Glycol, Carbomer, Fragrance, Tocopherol.

  • Package Labeling:

    Box6

  • INGREDIENTS AND APPEARANCE
    ELEMENT CONTROL RINSE FREE HAND SANITIZER SOOTHING 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79995-027
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.7 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79995-027-01500 mL in 1 BOTTLE; Type 0: Not a Combination Product06/25/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E06/25/2020
    Labeler - Strategic Orient Sourcing Limited (667569581)
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