Label: MOOR SPA HAND SANITIZING- ethanol liquid

  • NDC Code(s): 81441-008-01, 81441-008-02, 81441-008-03
  • Packager: Bodywell Natural Skin Ca re Inc
  • 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 January 17, 2023

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  • Drug facts

  • Active ingredient

    Ethanol 70%

  • Purpose

    Antiseptic

  • Uses

    Hand Sanitizer to Help reduce bacteria that potentially can cause disease. For use
    when soap and water are not available.

  • Warnings

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

        Do not use

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

    When using this product keep out of eyes, ears and mouth. In case of contact with eyes,
    rinse thoroughly with water.
    Stop use and ask a doctor if irritation occurs. These may be signs of a serious condition.

  • Keep out of reach of children.

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

  • Directions

    Spray enough product on hands to cover all surfaces. Rub hands together until dry.
    Supervise children under 6 year of age when using this product to avoid swallowing.

  • Other Information.

    • Store between 15-30 °C (59-86 °F)

    • Avoid freezing & excessive heat above 40°C (104°F)

  • Inactive Ingredients.

    Aqua, Aloe Barbadensis (Aloe Vera) Leaf Juice, Glycerin, D Alpha Tocopherol (Vitamin E), Western Red Cedar (Thuja Plicata) Leaf Oil

  • Product label

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  • INGREDIENTS AND APPEARANCE
    MOOR SPA HAND SANITIZING 
    ethanol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81441-008
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    .ALPHA.-TOCOPHEROL, D- (UNII: N9PR3490H9)  
    THUJA PLICATA LEAF (UNII: R9I752FESH)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:81441-008-01120 mL in 1 BOTTLE; Type 0: Not a Combination Product05/07/2021
    2NDC:81441-008-02500 mL in 1 BOTTLE; Type 0: Not a Combination Product05/07/2021
    3NDC:81441-008-033800 mL in 1 DRUM; Type 0: Not a Combination Product05/07/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A05/07/2021
    Labeler - Bodywell Natural Skin Ca re Inc (201162026)
    Establishment
    NameAddressID/FEIBusiness Operations
    Bodywell Natural Skin Care Inc201162026manufacture(81441-008)
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