Label: NATURES WILLOW BALM ITCH RELIEF CREAM- menthol cream

  • 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 1%

  • Purpose

    External Analgesic

  • Uses

    For the temporary relief of pain and itching associated with:

    - insect bites

    - minor skin irritations

    - scrapes

    - sunburn

  • Warnings

    For External use only

    Do not use on wounds or damaged skin

    When using this product

    • avoid contact wth eyes
    • do not bandage tightly

    Stop use and ask a dctor if

    • condition worsen
    • symptoms persist for more than 7 days sor clear up and occur again wthin 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 to 4 times daily

    Children under 2 years of age: consult a physician

  • Inactive Ingredients

    Almond Oil, Camphor, Caprylyl Glycol, Ceteareth-20, Cetearyl Alcohol, Cetyl Alcohol, Eucalyptus Oil, Geranium Oil, Glyceryl Stearate SE, Helichrysum Gymnocephalum Oil, Isopropyl Palmitate, Jojoba Seed Extract, Lavender Oil, Lemongrass Oil, Palmitic Acid, Phenoxyethanol, Propanediol, Sorbic Acid, Stearic Acid, Stearyl Alcohol, Sunflower Oil, Triethanolamine, Water, White Willow Bark Extract

  • SPL UNCLASSIFIED SECTION

    Distributed by WB Ventures LLC, Cincinnati, OH 45212

    For more information or to report a serious adverse event contact 1-888-609-4556

  • Packaging Label

    tube

  • INGREDIENTS AND APPEARANCE
    NATURES WILLOW BALM ITCH RELIEF CREAM 
    menthol cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73498-028
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL10 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    PELARGONIUM GRAVEOLENS FLOWER OIL (UNII: 3K0J1S7QGC)  
    SIMMONDSIA CHINENSIS SEED (UNII: D24K2Q1F6H)  
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)  
    STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
    LAVENDER OIL (UNII: ZBP1YXW0H8)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    HELICHRYSUM GYMNOCEPHALUM WHOLE (UNII: 0369G6I64W)  
    GLYCERYL STEARATE SE (UNII: FCZ5MH785I)  
    WEST INDIAN LEMONGRASS OIL (UNII: 5BIA40E9ED)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    SORBIC ACID (UNII: X045WJ989B)  
    SUNFLOWER OIL (UNII: 3W1JG795YI)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)  
    SALIX ALBA BARK (UNII: 205MXS71H7)  
    PALMITIC ACID (UNII: 2V16EO95H1)  
    WATER (UNII: 059QF0KO0R)  
    ALMOND OIL (UNII: 66YXD4DKO9)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73498-028-0199 g in 1 TUBE; Type 0: Not a Combination Product12/29/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01712/29/2023
    Labeler - WB Ventures LLC (067482664)