Active Ingredients
White Willow (Salix Alba bark)
White Cedar (Thuja Occidentalis leaf)
Willow Wart
FDA Label NDC 82309-032
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Tripak Pharmaceuticals for the product Willow Wart (NDC 82309-032). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredients, purpose, uses, warnings, otc - do not use, otc - pregnancy or breast feeding, otc - keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
White Willow (Salix Alba stem and bark)..........Wart and Skin tag remover
White Cedar (Thuja Occidentalis leaf)..............Wart and Skin tag remover
Uses
- For the removal of common warts (including plantar warts) and skin tags
Warnings
For external use only
Avoid contact with eyes
Otc - Do Not Use
Do not use on broken or irritated skin
If irritation develops discontinue use
Otc - Pregnancy Or Breast Feeding
If pregnant or breast feeding, ask a health professional before use
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed get medical help or contact a poison control centre right away.
Directions
- 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 Information
Store below 30C/86F
Inactive Ingredients
Purified Water, Apple Cider Vinegar, Alcohol, Lactic Acid, Filipendula Ulmaria Whole Plant, Glycerin, Acetic Acid, Potassium Sorbate, Santalum Spicatum (Sandalwood) Oil, Xanthan Gum
Box
82309-032-02 Box label
Tube
82309-033-01 Label
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