Label: SERVO STAT BAC- benzalkonium chloride liquid

  • 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 21, 2020

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  • ACTIVE INGREDIENT

    Benzalkonium Chloride 0.1%

  • INACTIVE INGREDIENT

    Water, Dihydroxy-propyl PEG-5-Linoleammonium Chloride, Glycereth-2 Cocoate, Behentrimonium Chloride, Dihdroxyethyl Cocamine Oxide.

  • WARNINGS

    For external use only - When using this product - do not get into eyes - if contact occurs, rinse eyes thoroughly with water - Stop use and ask a doctor if - irritation and redness ...

  • DOSAGE & ADMINISTRATION

    Apply to hands and rub lightly until dry without wiping or rinsing

  • INDICATIONS & USAGE

    USE FOR HAND-WASHING TO DECREASE BACTERIA ON THE SKIN

    If hands are visibly soiled, use regular soap and water
    Recommended for repeated use

  • KEEP OUT OF REACH OF CHILDREN

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

  • PURPOSE

    Antiseptic

  • PRINCIPAL DISPLAY PANEL

    3875ml NDC78041-0023

  • INGREDIENTS AND APPEARANCE
    SERVO STAT BAC 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:78041-0023
    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
    BEHENTRIMONIUM CHLORIDE (UNII: X7GNG3S47T)  
    DIHYDROXYETHYL COCAMINE OXIDE (UNII: 8AR51R3BL5)  
    GLYCERETH-2 COCOATE (UNII: JWM00VS7HC)  
    WATER (UNII: 059QF0KO0R)  
    DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE (UNII: 0Y0NQR2GH1)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:78041-0023-13875 mL in 1 BOTTLE; Type 0: Not a Combination Product07/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A07/01/2020
    Labeler - Fusion Chemcial (097714839)
    Registrant - Fusion Chemical (097714839)
    Establishment
    NameAddressID/FEIBusiness Operations
    Enzyme Solution004994559manufacture(78041-0023)
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