Label: WILLOW WART- salix alba, thuja occidentalis cream
- NDC Code(s): 82309-032-01, 82309-032-02
- Packager: Tripak Pharmaceuticals
- 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 December 18, 2023
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INGREDIENTS AND APPEARANCE
WILLOW WART
salix alba, thuja occidentalis creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82309-032 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength THUJA OCCIDENTALIS LEAF (UNII: 0T0DQN8786) (THUJA OCCIDENTALIS LEAF - UNII:0T0DQN8786) THUJA OCCIDENTALIS LEAF 0.2 g in 10 g SALIX ALBA BARK (UNII: 205MXS71H7) (SALIX ALBA BARK - UNII:205MXS71H7) SALIX ALBA BARK 0.5 g in 10 g Inactive Ingredients Ingredient Name Strength SANTALUM SPICATUM OIL (UNII: H9LVS6REV4) APPLE CIDER VINEGAR (UNII: 0UE22Q87VC) GLYCERIN (UNII: PDC6A3C0OX) ALCOHOL (UNII: 3K9958V90M) XANTHAN GUM (UNII: TTV12P4NEE) WATER (UNII: 059QF0KO0R) LACTIC ACID (UNII: 33X04XA5AT) FILIPENDULA ULMARIA WHOLE (UNII: 3LH0M209LN) ACETIC ACID (UNII: Q40Q9N063P) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82309-032-02 1 in 1 BOX 12/01/2021 1 NDC:82309-032-01 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 06/01/2019 Labeler - Tripak Pharmaceuticals (758658819)