SOMXL Homeopathic Wart Remover

Manufacturer
WR Group Skin Care Ltd
Effective date
2025-03-03
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
full-release
Hydrated at
2026-06-01 02:32:13

Label at a glance#

ProductSOMXL Homeopathic Wart Remover
Active ingredientTHUJA OCCIDENTALIS LEAFY TWIG
Label structure6 sections

Dosage and administration

•Wash affected area (May soak wart in warm water for 15-minutes if desired). • Dry area throughly. • Apply small amount with applicator to cover each wart. Let dry.  • Repeat this procedure once or twice daily as needed for up to 12-weeks.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

White cedar (Thuja occidentalis) 6X HPUS ...... The letters 'HPUS' indicate that the component in this product
is officially monographed in the Homoeopathic Pharmacopoeia of the United States

Purpose

OTC - PURPOSE SECTION

Wart Remover

Use

INDICATIONS & USAGE SECTION

For the removal of common warts. The common wart is easily recognized by the rough “cauliflower-like” appearance on the surface.

Warnings

WARNINGS SECTION

For external use only
If product gets into eyes, flush with water for 15-minutes. Avoid inhaling vapors.

Do not use

OTC - DO NOT USE SECTION

• on irritated skin • on any area that is infected or reddened • if you are diabetic or if you have poor blood circulation • miles • birthmarks • warts with hair growing from them • gential warts • warts on the face or mucous membranes

Stop use and ask a doctor if

OTC - STOP USE SECTION

discomfort persists

If pregnant or breast-feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

•Wash affected area (May soak wart in warm water for 15-minutes if desired). • Dry area throughly. • Apply small amount with applicator to cover each wart. Let dry.  • Repeat this procedure once or twice daily as needed for up to 12-weeks.

Inactive ingredients

INACTIVE INGREDIENT SECTION

DEIONIZED WATER, BIRCH OIL, C13-14 ISOPARAFFIN, HYDROGEN PEROXIDE, LAURETH-7, POLYACRYLAMIDE, SODIUM STANNATE

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
5eb9f24b-9328-475e-af0a-18021935eb6aProduct name120180220

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70463-725-01SOMXL Homeopathic Wart Remover15 g in 1 TUBECREAM157
70463-725-01SOMXL Homeopathic Wart Remover1 in 1 BOXCREAM17

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70463-725SOMXL HOMEOPATHIC WART REMOVER (THUJA OCCIDENTALIS LEAFY TWIG) CREAM [WR GROUP SKIN CARE LTD]7Current NDC, Legacy NDC, 2 package rows20250305_63e48a74-0efd-4ebe-a5c6-cbdfd6b9c0c8.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70463-72570463-725-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
SOMXL Homeopathic Wart RemoverTHUJA OCCIDENTALIS LEAFY TWIGWR Group Skin Care Ltd63e48a74-0efd-4ebe-a5c6-cbdfd6b9c0c82025-03-03WarningsExact identifier
ndc (package): 70463-725-01
ndc (product): 70463-725
ndc11 (package): 70463072501
spl id: 2f76aa11-04fe-8c60-e063-6294a90a5470
spl set id: 63e48a74-0efd-4ebe-a5c6-cbdfd6b9c0c8

Reported adverse events (FAERS/openFDA)#

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