Label: EMU HAND SANITIZER MIST OCEAN SURF- alcohol spray

  • NDC Code(s): 80464-1002-1
  • Packager: EVERYONE MUST USE, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 22, 2023

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  • Purpose

    Antiseptic, Hand Sanitizer

  • Drug Facts

    Active Ingredient

    Active IngredientPurpose
    Alcohol 80% v/v.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. | Contents under pressure.

    Do not use on children less than 2 months of age. Do not use on open skin wounds.

    When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

    Stop using and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

    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 to avoid swallowing.

  • Other information

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

  • Inactive ingredients

    Aloe, Fragrance, Glycerin, Purified Water, Vitamin E

  • Questions or comments?

    1-800-250-4643

  • Package Label - Principal Display Panel

    Net Wt 2.2 FL OZ (62.4g) NDC: 80464-1002-1

    Label

  • INGREDIENTS AND APPEARANCE
    EMU HAND SANITIZER MIST OCEAN SURF 
    alcohol spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80464-1002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.62 g  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    ALOE (UNII: V5VD430YW9)  
    WATER (UNII: 059QF0KO0R)  
    ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:80464-1002-162.4 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product09/21/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)09/21/2020
    Labeler - EVERYONE MUST USE, LLC (117650280)
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