Label: PURE CARE HAND SANITIZER- alcohol gel

  • NDC Code(s): 73928-004-01, 73928-004-02, 73928-004-03, 73928-004-04, view more
    73928-004-05, 73928-004-06
  • Packager: KINGKEY MBC LIFE TECHNOLOGY GROUP CO., LTD
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated October 29, 2024

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  • Active Ingredient

    Alcohol 75% v/v.

  • Purpose

    Antiseptic

  • Uses

    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.

    Do not use

    • in children less than 2 months of age
    • on open skin wounds

    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.

  • 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

    • Store between 59-86 0F (15-30 0C)
    • Avoid freezing and excecssive heat above 104 0F (40 0C)
  • Inactive ingredients

  • Package Label - Principal Display Panel

    Label

  • INGREDIENTS AND APPEARANCE
    PURE CARE HAND SANITIZER 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73928-004
    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)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73928-004-0159 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/26/2020
    2NDC:73928-004-02148 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/26/2020
    3NDC:73928-004-03236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/26/2020
    4NDC:73928-004-04500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/26/2020
    5NDC:73928-004-05946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/26/2020
    6NDC:73928-004-063785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/26/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00305/26/2020
    Labeler - KINGKEY MBC LIFE TECHNOLOGY GROUP CO., LTD (545349263)
    Establishment
    NameAddressID/FEIBusiness Operations
    KINGKEY MBC LIFE TECHNOLOGY GROUP CO., LTD545349263manufacture(73928-004)
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