Label: HANDOUT PROTECTION HAND SANITIZER- isopropyl alcohol liquid

  • NDC Code(s): 73928-012-01, 73928-012-02, 73928-012-03, 73928-012-04, view more
    73928-012-05, 73928-012-06, 73928-012-07, 73928-012-08, 73928-012-09, 73928-012-10, 73928-012-11, 73928-012-12, 73928-012-13, 73928-012-14, 73928-012-15, 73928-012-16, 73928-012-17, 73928-012-18, 73928-012-19, 73928-012-20, 73928-012-21, 73928-012-22, 73928-012-23, 73928-012-24, 73928-012-25, 73928-012-26
  • Packager: KINGKEY MBC LIFE TECHNOLOGY GROUP CO., LTD
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 29, 2024

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  • Active Ingredient

    lsopropyl Alcohol 75% v/v

  • Purpose

    Antiseptic

  • Use

    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

  • WHEN USING

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

    Stop use and ask a doctor ifirritation or rash occurs. These may be signs of a serious condition.

  • 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.

    Do not use
    • In children less than 2 months of age
    • On open skin wounds

  • Directions

    • Place enough product on hands to cover all surfaces. Rub hands together until dry.
    • Supervise children under 6 years of age when using this product to avoid swallowing.
  • Other information

    Do not store above 105F

  • Inactive ingredients

    aloe gel, condensed green tea, glycerin, Hydrogen peroxide

  • Package Label - Principal Display Panel

    Label

    Label

  • INGREDIENTS AND APPEARANCE
    HANDOUT PROTECTION HAND SANITIZER 
    isopropyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73928-012
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL75 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    HYDROGEN PEROXIDE (UNII: BBX060AN9V)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73928-012-011 mL in 1 POUCH; Type 0: Not a Combination Product09/28/2020
    2NDC:73928-012-022 mL in 1 POUCH; Type 0: Not a Combination Product09/28/2020
    3NDC:73928-012-033 mL in 1 POUCH; Type 0: Not a Combination Product09/28/2020
    4NDC:73928-012-044 mL in 1 POUCH; Type 0: Not a Combination Product09/28/2020
    5NDC:73928-012-055 mL in 1 POUCH; Type 0: Not a Combination Product09/28/2020
    6NDC:73928-012-066 mL in 1 POUCH; Type 0: Not a Combination Product09/28/2020
    7NDC:73928-012-077 mL in 1 POUCH; Type 0: Not a Combination Product09/28/2020
    8NDC:73928-012-088 mL in 1 POUCH; Type 0: Not a Combination Product09/28/2020
    9NDC:73928-012-099 mL in 1 POUCH; Type 0: Not a Combination Product09/28/2020
    10NDC:73928-012-1010 mL in 1 POUCH; Type 0: Not a Combination Product09/28/2020
    11NDC:73928-012-1130 mL in 1 BOTTLE; Type 0: Not a Combination Product09/28/2020
    12NDC:73928-012-1250 mL in 1 BOTTLE; Type 0: Not a Combination Product09/28/2020
    13NDC:73928-012-1360 mL in 1 BOTTLE; Type 0: Not a Combination Product09/28/2020
    14NDC:73928-012-14100 mL in 1 BOTTLE; Type 0: Not a Combination Product09/28/2020
    15NDC:73928-012-15150 mL in 1 BOTTLE; Type 0: Not a Combination Product09/28/2020
    16NDC:73928-012-16180 mL in 1 BOTTLE; Type 0: Not a Combination Product09/28/2020
    17NDC:73928-012-17200 mL in 1 BOTTLE; Type 0: Not a Combination Product09/28/2020
    18NDC:73928-012-18236 mL in 1 BOTTLE; Type 0: Not a Combination Product09/28/2020
    19NDC:73928-012-19250 mL in 1 BOTTLE; Type 0: Not a Combination Product09/28/2020
    20NDC:73928-012-20300 mL in 1 BOTTLE; Type 0: Not a Combination Product09/28/2020
    21NDC:73928-012-21350 mL in 1 BOTTLE; Type 0: Not a Combination Product09/28/2020
    22NDC:73928-012-22400 mL in 1 BOTTLE; Type 0: Not a Combination Product09/28/2020
    23NDC:73928-012-23450 mL in 1 BOTTLE; Type 0: Not a Combination Product09/28/2020
    24NDC:73928-012-24500 mL in 1 BOTTLE; Type 0: Not a Combination Product09/28/2020
    25NDC:73928-012-251000 mL in 1 BOTTLE; Type 0: Not a Combination Product09/28/2020
    26NDC:73928-012-262000 mL in 1 BOTTLE; Type 0: Not a Combination Product09/28/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00309/28/2020
    Labeler - KINGKEY MBC LIFE TECHNOLOGY GROUP CO., LTD (545349263)
    Establishment
    NameAddressID/FEIBusiness Operations
    KINGKEY MBC LIFE TECHNOLOGY GROUP CO., LTD545349263manufacture(73928-012)
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