Label: WILLOW WART- salix alba, thuja occidentalis cream

  • NDC Code(s): 50017-032-01, 50017-032-02
  • Packager: Neat Feat Products Limited
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved homeopathic

DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

Drug Label Information

Updated February 13, 2023

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

  • ACTIVE INGREDIENT

    White Willow (Salix Alba bark)

    White Cedar (Thuja Occidentalis leaf)

  • PURPOSE

    White Willow (Salix Alba stem and bark)..........Wart and Skin tag remover

    White Cedar (Thuja Occidentalis leaf)..............Wart and Skin tag remover

  • INDICATIONS & USAGE

    For the removal of common warts (including plantar warts) and skin tags

  • WARNINGS

    For external use only

    Avoid contact with eyes

    Do not use on broken or irritated skin

    If irritation develops discontinue use

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

    Keep out of reach of children. If swallowed get medical help or contact a poison control centre right away.

  • INACTIVE INGREDIENT

    Purified Water, Apple Cider Vinegar, Alcohol, Lactic Acid, Filipendula Ulmaria Whole Plant, Glycerin, Acetic Acid, Potassium Sorbate, Santalum Spicatum (Sandalwood) Oil, Xanthan Gum

  • DOSAGE & ADMINISTRATION

    Directly apply one or two drops at a time to completely cover the wart or skin tag
    For best results cover with a dressing/plaster or similar
    Repeat this procedure once or twice daily as needed

  • OTHER SAFETY INFORMATION

    Store below 30C/86F

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children

  • Willow Wart Label 10g

    50017-032-01

    Label 10g Box

  • INGREDIENTS AND APPEARANCE
    WILLOW WART 
    salix alba, thuja occidentalis cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50017-032
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALIX ALBA BARK (UNII: 205MXS71H7) (SALIX ALBA BARK - UNII:205MXS71H7) SALIX ALBA BARK0.5 g  in 10 g
    THUJA OCCIDENTALIS LEAF (UNII: 0T0DQN8786) (THUJA OCCIDENTALIS LEAF - UNII:0T0DQN8786) THUJA OCCIDENTALIS LEAF0.2 g  in 10 g
    Inactive Ingredients
    Ingredient NameStrength
    APPLE CIDER VINEGAR (UNII: 0UE22Q87VC)  
    LACTIC ACID (UNII: 33X04XA5AT)  
    WATER (UNII: 059QF0KO0R)  
    FILIPENDULA ULMARIA WHOLE (UNII: 3LH0M209LN)  
    SANTALUM SPICATUM OIL (UNII: H9LVS6REV4)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ALCOHOL (UNII: 3K9958V90M)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    ACETIC ACID (UNII: Q40Q9N063P)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:50017-032-021 in 1 BOX01/02/2023
    1NDC:50017-032-0110 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic01/02/2023
    Labeler - Neat Feat Products Limited (590412409)