Label: CARE TOUCH ANTIBACTERIAL HANDSOAP ROSE LAVENDER- benzalkonium chloride liquid

  • NDC Code(s): 70393-052-01
  • Packager: Future Diagnostics Llc
  • 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 August 31, 2020

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

  • Drug Facts

  • Active ingredient

    Benzalkonium chloride 0.1

  • PURPOSE

    Purpose................................Antibacterial

  • Uses

    For hand washing to decrease bacteria on the skin.

  • Uses

    For hand washing to decrease bacteria on the skin.

  • Warnings For external use only.

    Do not use
    • in the eyes.
    • if you are allergic to any of the ingredients.

    When using this product if eye contact occurs, rinse thoroughly with water.

    Stop use and ask a doctor if irritation or redness develops and persists.

    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 15 seconds

    • Wash skin, rinse thoroughly and dry

  • Inactive ingredient

    Aqua, Cocamidopropylamine Oxide, Glycerin, Cocamide Methyl MEA, Aloe Barbadensis Leaf Water, PEG-150 Distearate,

    Cetrimonium Chloride, Sodium Chloride, Phenoxyethanol, Disodium EDTA, Tocopheryl Acetate.

  • SPL UNCLASSIFIED SECTION

    KILLS 99.99% OF BACTERIA

    *kills 99.99% of most germs

    Made in China for Future Brands

    Brooklyn, NY 11220 1800.758.3830

    caretouchusa.com

  • Packaging

    IMAGE

  • INGREDIENTS AND APPEARANCE
    CARE TOUCH ANTIBACTERIAL HANDSOAP ROSE LAVENDER 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70393-052
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.1 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    COCAMIDOPROPYLAMINE OXIDE (UNII: M4SL82J7HK)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    COCOYL METHYL MONOETHANOLAMINE (UNII: 79G1T427CF)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)  
    CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70393-052-01400 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 finalpart333E09/01/2020
    Labeler - Future Diagnostics Llc (080113296)
    Establishment
    NameAddressID/FEIBusiness Operations
    Shenzhen Lantern Science Co., ltd.421222423manufacture(70393-052)