Label: FRESH SCENT HAND SANITIZER- ethyl alcohol liquid

  • Category: HUMAN OTC DRUG LABEL

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 February 8, 2019

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • ACTIVE INGREDIENT


    Active ingredients  

    Ethyl Alcohol 62.0%

  • PURPOSE


    Purpose  

    Antimicrobial

  • INDICATIONS & USAGE

    Use hand sanitizer
    to help reduce
    bacteria on skin.

  • WARNINGS

    Flammable  Keep

    away from heat and flame

  • WHEN USING

    When using this
    product avoid contact
    with eyes. If contact
    occurs, rinse
    thoroughly with water.

  • STOP USE

    Stop use and ask
    doctor if irritation or
    redness develops.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach
    of children.
    If swallowed, get
    medical help or
    contact a Poison
    Control center
    right away.

  • DOSAGE & ADMINISTRATION

    Directions
    ■ Wet hands
    thoroughly with
    product and rub
    into skin until dry.
    ■ Children under
    6 years of age
    should be
    supervised by an
    adult when using.


  • INACTIVE INGREDIENT

    Inactive
    Ingredients
    Water (Aqua), Aloe
    Barbadensis Leaf
    Juice, Carbomer,
    Fragrance, Glycerin,
    Propylene Glycol,
    Triethanolamine,
    Tocopheryl Acetate.

  • Principal Display Package

    FRESH SCENT
    HAND SANITIZER
    1 FL OZ (29 mL)

    PEEL UP TO SEE
    ADDITIONAL DRUG FACTS

    Distributed By:
    GL360, LLC
    Troy Michigan, 48084
    Made in China

    Product Package

    Captain America 9823-1

    3 29500 00196 7

    Baby Groot 9824-1

    3 29500 00195 0

    Captain Marvel 9825-1

    3 29500 00003 8

                                   FRESH SCENT HAND SANITIZER by GL360, LLC

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  • INGREDIENTS AND APPEARANCE
    FRESH SCENT HAND SANITIZER 
    ethyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:29500-9823
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL17.98 mL  in 29 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:29500-9823-129 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/01/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E01/01/2019
    FRESH SCENT HAND SANITIZER 
    ethyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:29500-9824
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL17.98 mL  in 29 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:29500-9824-129 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/01/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E01/01/2019
    FRESH SCENT HAND SANITIZER 
    ethyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:29500-9825
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL17.98 mL  in 29 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:29500-9825-129 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/01/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E01/01/2019
    Labeler - GL 360 (966155082)