Label: BOLISI DISPSABLE HAND SANITIZER- alcohol solution

  • 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 April 18, 2020

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  • Drug Facts

  • Active ingredient

    Ethyl Alcohol 75%±5% (V/V)

  • Purpose

     Antiseptic

  • Use

    hand sanitizer to help decrease bacteria on the skin and recommended for repeated use.

  • KEEP OUT OF REACH OF CHILDREN

    Children must be supervised in use of this product.

  • Warnings:

    • For external use only.
    • Flammable.
    • Keep away from fire or flame.
    • Do not apply around eyes.
    • Do not use in ears and mouth.

    When using this product, Avoid contact with eyes. In case of contact flush eyes with water.

    Stop use and ask a doctor if irritation or rash appears on the skin.

  • DOSAGE & ADMINISTRATION

    Place enough product in your palm to thoroughly cover your hands rub together briskly until dry.

    Children under 6 years of age should be supervised when using this product.

    Other Information: 

    • Do not store above 85℉.
    • May discolor certain fabrics or surfaces.
  • Inactive ingredients

    Water, Proplene Glycol, Triethanolamine, Carbomer.

  • Packaging

    image description

  • INGREDIENTS AND APPEARANCE
    BOLISI DISPSABLE HAND SANITIZER 
    alcohol solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75255-002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL75 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    water (UNII: 059QF0KO0R)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:75255-002-0160 mL in 1 BOTTLE; Type 0: Not a Combination Product04/14/2020
    2NDC:75255-002-02100 mL in 1 BOTTLE; Type 0: Not a Combination Product04/14/2020
    3NDC:75255-002-03250 mL in 1 BOTTLE; Type 0: Not a Combination Product04/14/2020
    4NDC:75255-002-04480 mL in 1 BOTTLE; Type 0: Not a Combination Product04/14/2020
    5NDC:75255-002-05100 mL in 1 TUBE; Type 0: Not a Combination Product04/15/2020
    6NDC:75255-002-06500 mL in 1 BOTTLE; Type 0: Not a Combination Product04/15/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E04/14/2020
    Labeler - Guangzhou Baoli Cosmetics Co., Ltd. (526940311)
    Registrant - Guangzhou Baoli Cosmetics Co., Ltd. (526940311)
    Establishment
    NameAddressID/FEIBusiness Operations
    Guangzhou Baoli Cosmetics Co., Ltd.526940311manufacture(75255-002)
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