Label: PIONEER ECLIPSE TOUCHE FOAMING NON-ALCOHOL HAND SANITIZER- benzalkonium chloride solution

  • 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 September 21, 2023

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  • Active ingredient

    BENZALKONIUM CHLORIDE  0.13%

    Purpose

    Antibacterial

  • Uses

    • For handwashing to reduce bacteria on the skin. Recommended for repeated use.
  • Warnings

    For external use only

    Avoid contact with eyes. In case of eye contact, flush eyes with water.

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

  • STOP USE

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

  • Directions

    • Apply foam sanitizer to hands.
    • Rub over surfaces of both hands for 15 seconds.
    • No rinsing required.
  • Inactive ingredients

    WATER, COCO-GLUCOSIDE, LAURTRIMONIUM CHLORIDE, COCAMIDOPROPYLAMINE OXIDE, CITRIC ACID, FRAGRANCE.

  • PRINCIPAL DISPLAY PANEL

    Pioneer_Non-Alcohol Hand Sanitizer_China

  • INGREDIENTS AND APPEARANCE
    PIONEER ECLIPSE TOUCHE FOAMING NON-ALCOHOL HAND SANITIZER 
    benzalkonium chloride solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70415-305
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    COCO GLUCOSIDE (UNII: ICS790225B)  
    LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC)  
    COCAMIDOPROPYLAMINE OXIDE (UNII: M4SL82J7HK)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70415-305-011000 mL in 1 BOTTLE; Type 0: Not a Combination Product08/04/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E08/04/2017
    Labeler - CWGC LA Inc. (034967904)
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