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
  • 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 February 12, 2021

If you are a consumer or patient please visit this version.

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

    Stop use and ask a doctor if irritation 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 not finalpart333A09/28/2020
    Labeler - KINGKEY MBC LIFE TECHNOLOGY GROUP CO., LTD (545349263)
    Establishment
    NameAddressID/FEIBusiness Operations
    KINGKEY MBC LIFE TECHNOLOGY GROUP CO., LTD545349263manufacture(73928-012)