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
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- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- INACTIVE INGREDIENT
- DOSAGE & ADMINISTRATION
- OTHER SAFETY INFORMATION
- KEEP OUT OF REACH OF CHILDREN
- Willow Wart Label 10g
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INGREDIENTS AND APPEARANCE
WILLOW WART
salix alba, thuja occidentalis creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50017-032 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALIX ALBA BARK (UNII: 205MXS71H7) (SALIX ALBA BARK - UNII:205MXS71H7) SALIX ALBA BARK 0.5 g in 10 g THUJA OCCIDENTALIS LEAF (UNII: 0T0DQN8786) (THUJA OCCIDENTALIS LEAF - UNII:0T0DQN8786) THUJA OCCIDENTALIS LEAF 0.2 g in 10 g Inactive Ingredients Ingredient Name Strength 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 Code Package Description Marketing Start Date Marketing End Date 1 NDC:50017-032-02 1 in 1 BOX 01/02/2023 1 NDC:50017-032-01 10 g in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 01/02/2023 Labeler - Neat Feat Products Limited (590412409)