Label: ARMOR ANTIBACTERIAL BODY TREATMENT BENZALKONIUM CHLORIDE- benzalkonium chloride liquid

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

Drug Label Information

Updated August 5, 2025

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  • Drug Facts

    Active ingredient

    Benzalkonium Chloride (0.13%)

  • Purpose

    Antiseptic

  • Uses

    • Helps reduce bacteria that can cause skin infections and odor
    • Deeply cleanses and detoxifies clogged pores
    • Ideal for acne-prone, oily, and sensitive skin
  • Warnings

    For external use only. Avoid contact with eyes. If contact occurs, rinse thoroughly with water

    Stop use and ask a doctorif irritation or redness develops and persists

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

  • KEEP OUT OF REACH OF CHILDREN

  • Directions

    • Apply to wet skin
    • Massage gently into a lather, focusing on problem areas
    • Rinse thoroughly
    • Use once or twice daily as needed
  • Inactive ingredients

    Water (Aqua), Cocamidopropyl Betaine, Sodium Lauroyl Sarcosinate, Glycerin, Charcoal Powder, Mel (Honey), Aloe Barbadensis Leaf Juice, Niacinamide, Panthenol, Butyrospermum Parkii (Shea) Butter, Chamomilla Recutita Flower Extract, Calendula Officinalis Extract, Cucumis Sativus (Cucumber) Fruit Extract, Tocopheryl Acetate, Allantoin, Citric Acid, Sodium Gluconate, Phenoxyethanol, Ethylhexylglycerin

  • Questions?

    • Store in a cool, dry place
    • Dermatologist tested
    • Free from parabens, sulfates, artificial dyes, and animal testing
    • Best if used within 12 months of opening
  • Product label

    image description

  • INGREDIENTS AND APPEARANCE
    ARMOR ANTIBACTERIAL BODY TREATMENT BENZALKONIUM CHLORIDE 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83004-028
    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)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    LOPERAMIDE (UNII: 6X9OC3H4II)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ACTIVATED CHARCOAL (UNII: 2P3VWU3H10)  
    HONEY (UNII: Y9H1V576FH)  
    ALOE VERA LEAF JUICE (UNII: RUE8E6T4NB)  
    NIACINAMIDE (UNII: 25X51I8RD4)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    SHEA BUTTER (UNII: K49155WL9Y)  
    CHAMOMILE FLOWER OIL (UNII: 60F80Z61A9)  
    CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)  
    CUCUMBER (UNII: YY7C30VXJT)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    ALLANTOIN (UNII: 344S277G0Z)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    SODIUM GLUCONATE (UNII: R6Q3791S76)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83004-028-01473 mL in 1 BOTTLE; Type 0: Not a Combination Product08/01/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00308/01/2025
    Labeler - Rida LLC (004425803)
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