Label: TARGET UP AND UP PAIN RELIEVING CLEANSING- benzalkonium chloride and lidocaine hydrochloride spray

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

Drug Label Information

Updated January 25, 2024

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  • Active Ingredients

    Benzalkonium Cl 0.13%

    Lidocaine HCL 2.5%

  • Purpose

    First aid antiseptic

    Pain relieving spray

  • Uses

    first aid to help prevent bacterial contamination or skin infection and for temporary relief of pain and itching associated with minor:

    • cuts
    • scrapes
    • minor burns
    • sunburn
    • minor skin irritations
  • Warnings

    For external use only

  • Ask a doctor before use if you have

    • deep or puncture wounds
    • animal bites
    • serious burns
  • When using this product

    • do not use in or near the eyes
    • do not apply over large areas of the body or in large quantities
    • do not apply over raw surfaces or blistered areas
  • Stop use and ask a doctor if

    • condition worsens
    • symptoms persist for more than 7 days, or clear up and occur again within a few days
  • Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • adults and children 2 years and older:
    • clean the affected area; apply a small amount on the area 1-3 times daily
    • may be covered with a sterile bandage
    • if bandaged, llet dry first
    • children under 2 years, ask a doctor
  • Other information

    • avoid excessive heat
    • store at room temperature
  • Inactive ingredients

    alcohol, disodium EDTA, fragrance, propylene glycol, purified water, sodium hydroxide

  • Label

    82938EF

  • INGREDIENTS AND APPEARANCE
    TARGET UP AND UP PAIN RELIEVING CLEANSING 
    benzalkonium chloride and lidocaine hydrochloride spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-252
    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
    LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS2.5 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    ALCOHOL (UNII: 3K9958V90M)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11673-252-21150 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product11/20/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00311/20/2023
    Labeler - TARGET CORPORATION (006961700)
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