Label: NATURES WILLOW ITCH RELIEF- menthol lotion

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

Drug Label Information

Updated December 19, 2023

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

  • Active ingredient

    Menthol 0.5%

  • Purpose

    External Analgeisc

  • Uses

    For the temporary relief of pain and itching associated with:

    • insect bites
    • minor skin irritations
    • scrapes
    • sunburn
  • Warnings

    For external use only.

    When using this product avoid contact with eyes.

    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

    If pregnant or breast-feeding, ask a health professional before use.

  • Keep out of reach of children

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • Adults and children over 2 years of age: apply to affected area not more than 3 times daily
    • Children under 2 years of age: consult a physician
  • Inactive ingredients

    1,2-Hexanediol, Camphor, Caprylhydroxamic Acid, Ceteareth-20, Cetearyl Alcohol, Cetyl Alcohol, Clary Oil, Eucalyptus Oil, Geranium Oil, Glyceryl Stearate, Helichrysum Gymnocephalum Oil, Jojoba Seed Oil, Lavender Oil, Propanediol, Sodium Hydroxide, Squalane, Stearic Acid, Stearyl Alcohol, Sunflower Seed Oil, Sweet Almond Oil, Water, White Willow Bark Extract

  • SPL Unclassified Section

    DISTRIBUTED BY WB VENTURES LLC

    COLD SPRING KY 41076

    FOR MORE INFORMATION OR TO REPORT A SERIOUS ADVERSE EVENT CONTACT 1-888-609-4556

    MADE IN CANADA

  • Package label

    Package Label

  • INGREDIENTS AND APPEARANCE
    NATURES WILLOW ITCH RELIEF 
    menthol lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73498-024
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL5 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERYL STEARATE SE (UNII: FCZ5MH785I)  
    JOJOBA OIL (UNII: 724GKU717M)  
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    HELICHRYSUM GYMNOCEPHALUM WHOLE (UNII: 0369G6I64W)  
    ALMOND OIL (UNII: 66YXD4DKO9)  
    CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)  
    WATER (UNII: 059QF0KO0R)  
    SALIX ALBA BARK (UNII: 205MXS71H7)  
    CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)  
    1,2-HEXANEDIOL (UNII: TR046Y3K1G)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    SUNFLOWER OIL (UNII: 3W1JG795YI)  
    LAVENDER OIL (UNII: ZBP1YXW0H8)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    CLARY SAGE OIL (UNII: 87L0D4U3M0)  
    SQUALANE (UNII: GW89575KF9)  
    STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
    POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    PELARGONIUM GRAVEOLENS FLOWER OIL (UNII: 3K0J1S7QGC)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73498-024-01226 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product04/20/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01703/30/202106/30/2024
    Labeler - WB Ventures LLC (067482664)