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

  • 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 December 3, 2021

If you are a consumer or patient please visit this version.

  • 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 not finalpart333A12/01/2018
    Labeler - Rite Aid Corporation (014578892)