Label: BACTINE MAX- bactine max wound wash liquid

  • NDC Code(s): 65197-820-80
  • Packager: WellSpring Pharmaceutical Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 29, 2020

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  • Active ingredient

    Benzalkonium Cl 0.13% w/w

  • Purpose

    First aid antiseptic

  • Use

    First aid to help prevent bacterial contamination or skin infection in minor cuts, scrapes and burns.

  • Warning

    For external use only. Do not use on or near the eyes. Do not apply to large areas of the body. Ask a doctor before use if -you have - deep or puncture wounds - animal bites - serious burns. Stop use and ask doctor if - condition persists or get worse - symptoms persist for more than 7 days.

    For external use only

    For external use only

    Do not use

    Ask a doctor before use if you have

    Ask a doctor or pharmacist before use if you are

    When using this product

    Stop use and ask a doctor if

    Pregnancy/breast-feeding warning

    Keep out of reach of children

  • Directions

    Clean the affected area, apply a small amount of this product on the area 1 to 3 times daily; may be covered with a sterile bandage (let dry first).

  • Other information

    Avoid excessive heat

  • Inactive ingredients

    aloe barbadensis leaf extract, edetate disodium, PEG-100 Stearate, propylene glycol, purified water

  • Questions?

    1-844-241-5454 Mon-Fri (8-5 EST) or bactine.com

  • Bactine Wound Wash Label

    Bactine Max Wound Wash IFC Label - CT82080B

    Bactine Max Wound Wash IFC Label


  • INGREDIENTS AND APPEARANCE
    BACTINE  MAX
    bactine max wound wash liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65197-820
    Route of AdministrationCUTANEOUS
    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
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    PEG-100 STEARATE (UNII: YD01N1999R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65197-820-801 in 1 CARTON04/15/2023
    1236 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00304/15/2023
    Labeler - WellSpring Pharmaceutical Corporation (110999054)
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