Willow Wart

Manufacturer: Tripak Pharmaceuticals
Effective date: 2023-12-18
Label type: HUMAN OTC DRUG LABEL
Version: 5
Source: full-release
Hydrated at: 2026-06-01 02:25:02

Label at a glance#

ProductWillow Wart

Active ingredientTHUJA OCCIDENTALIS LEAF, SALIX ALBA BARK

Label structure8 sections

Indications and uses

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

Dosage and 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

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

White Willow (Salix Alba bark)

White Cedar (Thuja Occidentalis leaf)

Purpose

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

OTC - DO NOT USE SECTION

Do not use on broken or irritated skin

If irritation develops discontinue use

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

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 Information

OTHER SAFETY INFORMATION

Store below 30C/86F

Inactive Ingredients

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

Box

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

82309-032-02 Box label label

Tube

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

82309-033-01 Label label

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
f52be47f-7aa7-46c0-b1fa-50c18dd50206	Product name	1	20201029
444b3e50-f226-46ef-bfca-2e7035d140cd	Product name	1	20190611
7cda52fc-125f-421c-8fea-bc1974370c49	Product name	2	20180703
48747306-602a-42cc-957b-5b0c69158eee	Product name	1	20180604
597b1cfd-7b31-5048-62be-ca5cd740da2f	Product name	1	20140508
db5ebcdb-b6ae-21cd-4dc5-76cd84b5578b	Product name	1	20140508
ec2149b3-5c6d-5344-f757-c86411073075	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
82309-032-02	2025-01-30	C162847	48780-1	f386c64a-3396-0266-e053-dadaa90a7c1a	Willow Wart
82309-032-02	2023-12-18	C162847	48780-1	f386c64a-3396-0266-e053-dadaa90a7c1a	Willow Wart
82309-032-02	2023-01-30	C162847	48780-1	f386c64a-3396-0266-e053-dadaa90a7c1a	Willow Wart

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
82309-032-01	Willow Wart	10 g in 1 TUBE	CREAM	10		5
82309-032-02	Willow Wart	1 in 1 BOX	CREAM	1		5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
82309-032	WILLOW WART (SALIX ALBA, THUJA OCCIDENTALIS) CREAM [TRIPAK PHARMACEUTICALS]	5	Legacy NDC, 2 package rows	20231219_d2185a5a-fc6f-c816-e053-2995a90ae496.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 14 matching rows.

Willow Wart
Salix alba, Thuja occidentalis
SANTALUM SPICATUM OIL
THUJA OCCIDENTALIS LEAF
SALIX ALBA BARK
APPLE CIDER VINEGAR
GLYCERIN
ALCOHOL
XANTHAN GUM
WATER
LACTIC ACID
FILIPENDULA ULMARIA WHOLE
ACETIC ACID
POTASSIUM SORBATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
82309-032	82309-032-01, 82309-032-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
SANTALUM SPICATUM OIL	H9LVS6REV4	IACT
THUJA OCCIDENTALIS LEAF	0T0DQN8786	ACTIB
SALIX ALBA BARK	205MXS71H7	ACTIB
APPLE CIDER VINEGAR	0UE22Q87VC	IACT
GLYCERIN	PDC6A3C0OX	IACT
ALCOHOL	3K9958V90M	IACT
XANTHAN GUM	TTV12P4NEE	IACT
WATER	059QF0KO0R	IACT
LACTIC ACID	33X04XA5AT	IACT
FILIPENDULA ULMARIA WHOLE	3LH0M209LN	IACT
ACETIC ACID	Q40Q9N063P	IACT
POTASSIUM SORBATE	1VPU26JZZ4	IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
0cca5b7e-5e79-65f8-e063-6294a90a13e7			d2185a5a-fc6f-c816-e053-2995a90ae496	2023-12-18	Warnings	Exact identifier spl id: 0cca5b7e-5e79-65f8-e063-6294a90a13e7 spl set id: d2185a5a-fc6f-c816-e053-2995a90ae496

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.