Label: ALCOHOL HAND SANITIZER gel

  • NDC Code(s): 74047-002-01, 74047-002-02, 74047-002-03, 74047-002-04, view more
    74047-002-05, 74047-002-06, 74047-002-07, 74047-002-08, 74047-002-09, 74047-002-10, 74047-002-11, 74047-002-12, 74047-002-13, 74047-002-14, 74047-002-15, 74047-002-16, 74047-002-17, 74047-002-18
  • Packager: Shantou Kangjie Daily Chemical Industry Co.,Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 11, 2023

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  • Active Ingredient

    Ethyl Alcohol 75%

  • Purpose

    Antimicrobial

  • Uses

    Hand Sanitizer to help reduce bacteria on skin.

  • WARNINGS

    Flammable.Keep away from fire or flame.For external use only.When using this product,do not use in or near the eyes.In case of contact,rinse eyes thoroughly with water.Stop use and ask doctor if irritation or rash appears and lasts.Keep out of reach for children. If swallowed, get medical help or contact a Poison Control Center right away.

  • DO NOT USE

    do not use in nesr the eyes. In case of contact, rinse eyes thoroughly with water

  • WHEN USING

    hen using this product,

    do not use in nesr the eyes. In case of contact, rinse eyes thoroughly with water

    Stop use and ask doctor if Irrtation or rash appears and lasts

    Keep out of resch for children. If Swallowed, get medical help or contact a Poison Conter right away

  • STOP USE

    Stop use and ask doctor if Irrtation or rash appears and lasts

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of resch for children. If Swallowed, get medical help or contact a Poison Conter right away

  • Directions

    Place enough Product in your palm to thoroughly spread on both hands and rub into the skin until dry.

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

  • Other Information

    Store below 106°F.(41℃)

    May discolor certain fabrics or surfaces.

  • INACTIVE INGREDIENTS

    Water, Carbomer, Wormwood Leaf Extract, dandelion extract, winter flower extract, Ammomethylpropanol

  • Package Label - Principal Display Panel

    74047-002-11 50ml TUBE74047-002-12 60ml74047-002-13 100ml TUBE74047-002-14 100ML74047-002-15 3780ml74047-002-16 19000mL74047-002-17 20000mL74047-002-18 25000mL74047-002-09 5L74047-002-02 30ml74047-002-03 50ml74047-002-05 236ml74047-002-06 250ml74047-002-07 500ml74047-002-08 1000ml74047-002-04 100ML74047-002-01 30 ML 74047-002-10 ROSEWOOD 30ML

  • INGREDIENTS AND APPEARANCE
    ALCOHOL HAND SANITIZER 
    alcohol hand sanitizer gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74047-002
    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)  
    CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)  
    ARTEMISIA ARGYI LEAF (UNII: 2JYC99Q0WZ)  
    BLACKBACK FOUNDER (UNII: PX3N99X6C9)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    TARAXACUM OFFICINALE ROOT (UNII: 9DE5YCO0RU)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:74047-002-0130 mL in 1 BOTTLE; Type 0: Not a Combination Product04/16/2020
    2NDC:74047-002-06250 mL in 1 BOTTLE; Type 0: Not a Combination Product04/16/2020
    3NDC:74047-002-07500 mL in 1 BOTTLE; Type 0: Not a Combination Product04/16/2020
    4NDC:74047-002-081000 mL in 1 BOTTLE; Type 0: Not a Combination Product04/16/2020
    5NDC:74047-002-0230 mL in 1 BOTTLE; Type 0: Not a Combination Product04/16/2020
    6NDC:74047-002-0350 mL in 1 BOTTLE; Type 0: Not a Combination Product04/16/2020
    7NDC:74047-002-04100 mL in 1 BOTTLE; Type 0: Not a Combination Product04/16/2020
    8NDC:74047-002-05236 mL in 1 BOTTLE; Type 0: Not a Combination Product04/16/2020
    9NDC:74047-002-095000 mL in 1 BOTTLE; Type 0: Not a Combination Product04/16/2020
    10NDC:74047-002-1030 mL in 1 BOTTLE; Type 0: Not a Combination Product04/16/2020
    11NDC:74047-002-1150 mL in 1 TUBE; Type 0: Not a Combination Product04/16/2020
    12NDC:74047-002-13100 mL in 1 TUBE; Type 0: Not a Combination Product04/16/2020
    13NDC:74047-002-14100 mL in 1 BOTTLE; Type 0: Not a Combination Product04/16/2020
    14NDC:74047-002-1260 mL in 1 BOTTLE; Type 0: Not a Combination Product04/16/2020
    15NDC:74047-002-1619000 mL in 1 BOTTLE; Type 0: Not a Combination Product04/16/2020
    16NDC:74047-002-1720000 mL in 1 BOTTLE; Type 0: Not a Combination Product04/16/2020
    17NDC:74047-002-1825000 mL in 1 BOTTLE; Type 0: Not a Combination Product04/16/2020
    18NDC:74047-002-153780 mL in 1 BOTTLE; Type 0: Not a Combination Product04/16/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00304/16/2020
    Labeler - Shantou Kangjie Daily Chemical Industry Co.,Ltd (527128712)
    Registrant - Shantou Kangjie Daily Chemical Industry Co.,Ltd (527128712)
    Establishment
    NameAddressID/FEIBusiness Operations
    Shantou Kangjie Daily Chemical Industry Co.,Ltd527128712manufacture(74047-002)
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