Label: LANACANE MAXIMUM STRENGTH ANTI-ITCH- benzethonium chloride and benzocaine cream

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

Drug Label Information

Updated November 29, 2023

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

  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • ACTIVE INGREDIENT

    Active ingredientsPurpose
    Benzethonium chloride 0.2%First-aid antiseptic
    Benzocaine 20%Pain relief cream
  • Uses

    first aid for the temporary relief of pain and itching and to help prevent infection in minor cuts, scrapes and burns

  • Warnings

    For external use only

    Do not use

    • in the eyes
    • over large areas of the body

    Ask a doctor before use if you have

    • deep or puncture wounds
    • animal bites
    • serious burns

    Stop use and ask a doctor if

    • condition worsens
    • needed for longer than 1 week

    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 of age and older: clean the affected area and apply a small amount to the affected area not more than 1 to 3 times daily
    • children under 2 years of age: ask a doctor
    • may be covered with a sterile bandage
  • Other information

    • store at 20-25°C (68-77°F)
    • retain carton for future reference
  • Inactive ingredients

    acetylated lanolin alcohol, aloe, cetyl acetate, cetyl alcohol, cholecalciferol, corn oil, dimethicone, dl-alpha tocopherol acetate, fragrance, glycerin, glyceryl monostearate, isopropyl myristate, methylparaben, mineral oil, PEG-100 stearate, polyvinylpyrrolidone/eicosene copolymer, propylparaben, pyrithione zinc, retinyl palmitate, sorbitan monostearate, stearamidopropyl PG-dimonium chloride phosphate, water

  • Questions?

    1-866-252-5327.

    You may also report side effects to this phone number.

  • SPL UNCLASSIFIED SECTION

    Distributed by: RB Health (US)
    Parsippany, NJ 07054-0224

  • PRINCIPAL DISPLAY PANEL - 28 g Tube Carton

    NDC 63824-810-01

    LANACANE ®

    Maximum Strength

    ANTI-ITCH
    CREAM

    Benzethonium chloride 0.2%
    (First-Aid Antiseptic)
    Benzocaine 20%
    (Pain Relieving Cream)

    2-in-1

    FAST Acting
    Itch Relief

    +

    Kills Germs*
    *unlike Hydrocortisones

    Temporary itch relief from:

    • Insect bites
    • Rashes
    • Dry, Itchy skin

    NET WT. 1 OZ (28 g)

    PRINCIPAL DISPLAY PANEL - 28 g Tube Carton
  • INGREDIENTS AND APPEARANCE
    LANACANE  MAXIMUM STRENGTH ANTI-ITCH
    benzethonium chloride and benzocaine cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63824-810
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP) BENZETHONIUM CHLORIDE2 mg  in 1 g
    BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE200 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    ACETYLATED LANOLIN ALCOHOLS (UNII: SNN716810P)  
    ALOE (UNII: V5VD430YW9)  
    CETYL ACETATE (UNII: 4Q43814HXS)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    CHOLECALCIFEROL (UNII: 1C6V77QF41)  
    CORN OIL (UNII: 8470G57WFM)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    PEG-100 STEARATE (UNII: YD01N1999R)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    PYRITHIONE ZINC (UNII: R953O2RHZ5)  
    SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)  
    STEARAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: W6000VEI5Y)  
    VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63824-810-011 in 1 CARTON09/28/201208/25/2025
    128 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00309/28/201208/25/2025
    Labeler - RB Health (US) LLC (081049410)