Label: FLAWLESS HAND SANITIZER- propolis extract spray

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated May 15, 2020

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  • ACTIVE INGREDIENT

    Propolis Extract 0.5%

  • INACTIVE INGREDIENTS

    Water, Sodium Silicate

  • PURPOSE

    Sanitizer

  • WARNINGS

    ■ For external use only.
    --------------------------------------------------------------------------------------------------------
    When using this product
    ■ Do not use in or near the eyes. In case of contact, rinse eyes thoroughly
    with water.
    ■ Avoid contact with broken skin.
    ■ Do not inhale or ingest.
    --------------------------------------------------------------------------------------------------------
    Stop use and ask a doctor
    ■ If irritation or rash appears and lasts.

  • KEEP OUT OF REACH OF CHILDREN

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

  • Uses

    ■ Hand sanitizer to help reduce bacteria that potentially can cause disease.
    ■ For use when soap and water are not available.

  • Directions

    ■ Please spray it at a distance of 10~20cm so that your hands are enough covered. Rub hands together until dry.
    ■ Supervise children under 6 years of age when using this product to avoid swallowing.

  • Other information

    ■ Store between 41~86℉(Between 5~30℃)
    ■ Avoid freezing and excessive heat above 104℉(40℃) and direct sunlight.

  • QUESTIONS

    ■ www.nbio.kr / 82-31-432-5670

  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    Image of bottle

  • INGREDIENTS AND APPEARANCE
    FLAWLESS HAND SANITIZER 
    propolis extract spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:77560-010
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PROPOLIS WAX (UNII: 6Y8XYV2NOF) (PROPOLIS WAX - UNII:6Y8XYV2NOF) PROPOLIS WAX1.25 g  in 250 mL
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Sodium Silicate (UNII: IJF18F77L3)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:77560-010-01250 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product05/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other05/01/2020
    Labeler - NBIO CO., LTD. (687218375)
    Registrant - NBIO CO., LTD. (687218375)
    Establishment
    NameAddressID/FEIBusiness Operations
    NBIO CO., LTD.687218375manufacture(77560-010)
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