Label: TSONG ANTI BACTERIAL FOAMING HAND WASH- benzalkonium chloride liquid

  • NDC Code(s): 79035-001-01
  • Packager: Tianjin Power-Long Packaging Technology Development Co.,Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 7, 2023

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  • Drug Facts

  • Active Ingredients

    Benzalkonium Chloride 0.13%

    Purpose

    Antiseptic

  • Use

    Hand wash to help reduce bacteria on skin; Recommended for daily use.

  • Warnings

    For external use only

    Do not apply around eyes.

    Do not use 

    in ears & mouth

    When using this product,

    avoid contact with eyes. In case of contact, flush eyes with water.

    Stop use and ask a doctor if

    redness or irritation develop and persist for more than 72 hours.

    Keep out of reach of children.

    Children must be supervised in use of this product.

  • Directions

    Apply appropriate amount to hands, massage generously to create a rich lather; Rinse thoroughly.

  • Other information

    Store at 20°C (68°F to 77°F), may discolor fabrics.

  • Inactive ingredients

    Water, Cetyltrimethylammonium Chloride, Cocoamidopropyl Betaine, Cocamide Methyl MEA, Sodium Chloride, Fragrance, Citric Acid,  Methylisothiazolinone, Methylchloroisothiazolinone.

  • Package Labeling: 300ml

    1

  • INGREDIENTS AND APPEARANCE
    TSONG ANTI BACTERIAL FOAMING HAND WASH 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79035-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    COCOYL METHYL MONOETHANOLAMINE (UNII: 79G1T427CF)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79035-001-01300 mL in 1 BOTTLE; Type 0: Not a Combination Product06/05/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)06/05/2020
    Labeler - Tianjin Power-Long Packaging Technology Development Co.,Ltd. (560220424)
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