Willow Wart

Manufacturer
Neat Feat Products Limited
Effective date
2025-01-08
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 02:30:09

Key Label Information#

Active Ingredients And Purpose

OTC - ACTIVE INGREDIENT SECTION

White Willow (Salix Alba bark) White Cedar (Thuja Occidentalis leaf)

OTC - PURPOSE SECTION

White Willow (Salix Alba stem and bark)..........Wart and Skin tag remover White Cedar (Thuja Occidentalis leaf)..............Wart and Skin tag remover

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

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.

Directions And Dosage

DOSAGE & ADMINISTRATION SECTION

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 Label Information

INACTIVE INGREDIENT SECTION

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

Willow Wart Label 10g

50017-032-01

Label Images#

Final revision Nov 2019 Willow Wart_10g Box_USA_FA
Final revision Nov 2019 Willow Wart_10g Box_USA_FA

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
48747306-602a-42cc-957b-5b0c69158eeeProduct name120180604
597b1cfd-7b31-5048-62be-ca5cd740da2fProduct name120140508
db5ebcdb-b6ae-21cd-4dc5-76cd84b5578bProduct name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50017-032WILLOW WART (SALIX ALBA, THUJA OCCIDENTALIS) CREAM [NEAT FEAT PRODUCTS LIMITED]6Legacy NDC20250110_897dcd1a-8fea-7bbf-e053-2995a90a185e.zip

Products#

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50017-03250017-032-01, 50017-032-02

Ingredients#

Complete SPL Sections#

OTC - ACTIVE INGREDIENT SECTION

OTC - ACTIVE INGREDIENT SECTION

White Willow (Salix Alba bark) White Cedar (Thuja Occidentalis leaf)

OTC - PURPOSE SECTION

OTC - PURPOSE SECTION

White Willow (Salix Alba stem and bark)..........Wart and Skin tag remover White Cedar (Thuja Occidentalis leaf)..............Wart and Skin tag remover

INDICATIONS & USAGE SECTION

INDICATIONS & USAGE SECTION

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

WARNINGS SECTION

WARNINGS SECTION

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 SECTION

INACTIVE INGREDIENT SECTION

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 SECTION

DOSAGE & ADMINISTRATION SECTION

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

OTHER SAFETY INFORMATION

Store below 30C/86F

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

Willow Wart Label 10g

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

50017-032-01

Source Document#

Source XML