Label: NOXYDERM- benzalkonium chloride liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 27, 2023

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  • Active Ingredient

    Active IngredientPurpose
    Benzalkonium Chloride 0.13%First Aid Antiseptic

  • Purpose

    Purpose

    First aid antiseptic

    Uses: first aid to help prevent infection in minor:

    • cuts
    • scrapes
    • burns
  • Do not use

    Do not use

    • in the eyes
    • over large areas of the body
    • longer than 1 week unless directed by a doctor

    Ask a doctor before use if you have

    • deep or pucture wounds, animal bites, or serious burns
  • Warnings For external use only

    Warnings

    For external use only

  • Keep out of reach of children

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

  • Instructions for use

    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
    • If bandaged, let dry first
  • Other safety information

    Store at room temperature

  • Dosage

    • Apply a small amount of this product on the area 1 to 3 times daily
  • Inactive ingredients

    Sodium Nitrite

    CoCo Betaine

    Deionized Water

    Citric Acid

  • INDICATIONS & USAGE

    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
    • If bandaged, let dry first
  • Warnings

    Warnings:

    For external use only

  • Questions

    Questions? call 1-888-585-4120

  • NOxyDERM

    NDC83823-001-01NDC83823-001-01

  • INGREDIENTS AND APPEARANCE
    NOXYDERM 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83823-001
    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
    COCO-BETAINE (UNII: 03DH2IZ3FY)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    SODIUM NITRITE (UNII: M0KG633D4F)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83823-001-01100 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product01/05/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00301/05/2024
    Labeler - NOxy Health Products (119031427)
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