Label: THE SPATHECARY FOAMING LAVENDER- benzalkonium chloride 0.13% soap

  • 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 October 13, 2020

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  • Active Ingredient

    Benzalkonium Chloride 0.13%

  • Purpose

    Antibacterial

  • Uses

    to help reduce bacteria that potentially can cause disease.

  • Warnings

    For external use only.

  • When using this product

    When using this product. Avoid contact with eyes. In case of eye contact, 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.

    If swallowed, get medical help or contact a Poison Control Center right away

  • Directions

    Pump into hands, wet as needed. Lather vigorously for at least 20 seconds. Wash skin, rinse thoroughly, and dry.

  • Other Information

    Store between 15-30C (59-86F)

  • Inactive Ingredients

    aqua/water/EAU, Sodium Laureth Sulfate, cocamidopropylamine oxide, cocamidopropyl betaine, glycerin, parfum, methylchloroisothiazolinone, Methylisothiazolinone, Magnesium chloride, Magnesium nitrate, Aloe Barbadensis Leaf Juice, Disodium EDTA, Citric Acid, Tocopheryl Acetate, FD &C yellow No.5 (CI 19140), FD&C Red No. 33 (CI 17200), FD&C Blue No. 1 (CI 42090)

  • Questions or Comments?

    P.O. Box 230258, Brooklyn, NY 11223

  • The Spathecary Foaming Hand Soap Lavender

    label

  • INGREDIENTS AND APPEARANCE
    THE SPATHECARY FOAMING LAVENDER 
    benzalkonium chloride 0.13% soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73166-111
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.65 g  in 500 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    MAGNESIUM NITRATE (UNII: 77CBG3UN78)  
    MAGNESIUM CHLORIDE ANHYDROUS (UNII: 59XN63C8VM)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER (UNII: 059QF0KO0R)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
    DISODIUM EDTA-COPPER (UNII: 6V475AX06U)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    COCAMIDOPROPYLAMINE OXIDE (UNII: M4SL82J7HK)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73166-111-16500 mL in 1 BOTTLE; Type 0: Not a Combination Product09/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A09/01/2020
    Labeler - Larry (Xiamen) Hi Tech Co., Ltd (529759328)
    Registrant - G2 Beauty Inc (124608169)
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