Label: 3 IN 1 FIRST AID WOUND CARE- benzethonium chloride solution

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

Drug Label Information

Updated November 22, 2023

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  • Drug Facts

  • Active ingredients

    Benzethonium Chloride 0.13%

    Purpose

    First aid Antiseptic

  • Uses

    First aid to help prevent the risk of bacterial contamination in minor cuts, scrapes and burns.

  • Warnings

    For external use only

    Do not use

    • in the eyes or apply over large areas of the body
    • longer than 1 week, unless directed by a doctor
    • for single patient use only

    Ask a doctor before use if you have

    • deep or punture wounds, animal bites or serious burns

    When using this product

    • do not puncture or incinerate
    • contents under pressure

    Stop use and consult a doctor if

    • condition persists or gets worse

    Keep out of reach of children

  • Directions

    • clean the affected area
    • spray a small amount of this product on the area 1 to 3 times a day
    • may be covered with a sterile bandage
    • if bandaged, let dry first
  • Other information

    • Store between 59° and 86° F (15° and 30° C).
    • See bottom of can for lot # and expiration date
  • Inactive ingredients

    aloe barbadensis leaf extract (aloe vera), benzalkonium chloride, maltodextrin, purified water, sodium bicarbonate, sodium chloride

  • Questions?

    1-888-547-5492

  • Package Labeling:

    Label

  • INGREDIENTS AND APPEARANCE
    3 IN 1 FIRST AID WOUND CARE 
    benzethonium chloride solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11822-5074
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP) BENZETHONIUM CHLORIDE1.3 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11822-5074-1211 g in 1 BOTTLE; Type 0: Not a Combination Product12/01/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)12/01/2018
    Labeler - Rite Aid Corporation (014578892)
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