Terrasil FAST AND NATURAL WART REMOVAL

Manufacturer
Aidance Skincare & Topical Solutions, LLC
Effective date
2024-05-24
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 21:01:20

Label at a glance#

ProductTerrasil FAST AND NATURAL WART REMOVAL MAXIMUM STRENGTH
Active ingredientTHUJA OCCIDENTALIS WHOLE
Label structure8 sections

Indications and uses

For the treatment of warts.

Dosage and administration

Wash and dry affected skin. Apply a layer of ointment and cover with a bandage as needed. Repeat procedure 2 times daily until skin improves. Store at room temperature. May stain fabrics.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Thuja 3X HPUS

The letters HPUS indicate the component(s) in this product is (are) officially monographed in the Homeopathic Pharmacopeia of the United States.

Purpose

OTC - PURPOSE SECTION

Wart Symptom Relief.

Uses

INDICATIONS & USAGE SECTION

For the treatment of warts.

Warnings

WARNINGS SECTION

For external use only. Ask a doctor before useif pregnant or nursing. When using this product, do not get into eyes.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, call poison control or seek medical help.

Directions

DOSAGE & ADMINISTRATION SECTION

Wash and dry affected skin. Apply a layer of ointment and cover with a bandage as needed. Repeat procedure 2 times daily until skin improves. Store at room temperature. May stain fabrics.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

beeswax, cedarwood oil, cottonseed oil, jojoba oil, magnesium oxide, silver stearate, zinc oxide.

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

14g Tube14g Tube50g Tube50g Tube

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
24909-186TERRASIL FAST AND NATURAL WART REMOVAL MAXIMUM STRENGTH (THUJA OCCIDENTALIS) OINTMENT [AIDANCE SKINCARE & TOPICAL SOLUTIONS, LLC]5Legacy NDC20240604_d768b51b-b989-47b4-b9fa-97fc04a42e70.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
24909-18624909-186-50, 24909-186-14

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
39b1f497-25c2-d82c-e063-6394a90ad1f5d768b51b-b989-47b4-b9fa-97fc04a42e702025-07-11WarningsExact identifier
spl set id: d768b51b-b989-47b4-b9fa-97fc04a42e70

Reported adverse events (FAERS/openFDA)#

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