Label: DG HEALTH MAXIMUM STRENGTH PAIN RELIEVING CLEANSING- benzalkonium cl, lidocaine hcl spray

  • NDC Code(s): 75712-200-01
  • Packager: Dollar General Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 17, 2024

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  • Active ingredients

    Benzalkonium Cl 0.13%

    Lidocaine HCl 4%

  • Purpose

    Benzalkonium Cl – First Aid Antiseptic

    Lidocaine HCl – 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
    • burns
    • sunburn
    • 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; spray a small amount on the area 1-3 times daily; may be covered with a sterile bandage (let dry first)
    • children under 2 years: ask a doctor
  • Other Safety Information

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

    chlorphenesin, edetate disodium, fragrance, glycerin, nonoxynol 9, phenoxyethanol, propylene glycol, purified water

  • Questions

    888-309-9030

  • Package/Label Principal Display Panel

    Label Front
  • Principal Display Panel

    Label Back
  • INGREDIENTS AND APPEARANCE
    DG HEALTH  MAXIMUM STRENGTH PAIN RELIEVING CLEANSING
    benzalkonium cl, lidocaine hcl spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75712-200
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
    LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS40 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    CHLORPHENESIN (UNII: I670DAL4SZ)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    NONOXYNOL-9 (UNII: 48Q180SH9T)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:75712-200-01148 mL in 1 BOTTLE; Type 0: Not a Combination Product02/11/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01702/11/2022
    Labeler - Dollar General Corporation (006946172)
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