Label: CARETOUCH ALCOHOL-FREE FOAMING HAND SANITIZER- benzalkonium chloride liquid

  • NDC Code(s): 70393-456-01, 70393-456-04, 70393-456-08, 70393-456-25
  • 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 March 15, 2020

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  • Drug Facts

  • Active ingredient

    Benzalkonium chloride 0.1%

  • Purpose

    Antibacterial

  • Uses

    • For hand washing to decrease bacteria on the skin.

  • Warnings

    For external use only.

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

    Stop use and ask a doctor if irritation or redness develops and persist for more than 72 hours.

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • Apply small amount of foam to hands as desired, allow drying without wiping.

  • Storage

    • Store at room temperature

    • Avoid direct sunlight.

  • Inactive ingredient

    Water, Betaine Anhydrous, Diazolidinyl urea, Phenoxyethanol, Palmitamidopropyltrimonium Chloride, Propylene Glycol, Sodium Citrate

  • SPL UNCLASSIFIED SECTION

    Alcohol-Free Moisturizing Formula

    Kills 99.99% of Germs*

    Fragrance-Free & Hypoallergenic

    Free of Triclosan, Parabens, Sulfates, Phthalates

    *Kills 99.99% of common, harmful germs in just 15 seconds.

    NDC 70393-456-25

    ITEM# CTAFF10

    NDC 70393-456-04

    ITEM# CTAFF10-4

    NDC 70393-456-01

    ITEM# CTAFFS-T1

    1800.758.3830

    caretouchusa.com

    Manufactured in China for Future Brands Brooklyn, NY 11220

  • Packaging

    sanitize1

  • INGREDIENTS AND APPEARANCE
    CARETOUCH ALCOHOL-FREE FOAMING HAND SANITIZER 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70393-456
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    BETAINE (UNII: 3SCV180C9W)  
    DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    PALMITAMIDOPROPYLTRIMONIUM CHLORIDE (UNII: N2U96D202F)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70393-456-25300 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/01/2019
    2NDC:70393-456-044 in 1 BAG03/01/2019
    2NDC:70393-456-25300 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    3NDC:70393-456-0150 mL in 1 BOTTLE; Type 0: Not a Combination Product03/15/2020
    4NDC:70393-456-088 in 1 PACKAGE03/15/2020
    4NDC:70393-456-0150 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A03/01/2019
    Labeler - Future Diagnostics Llc (080113296)
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