SkinTek Skin Tag Remover

Manufacturer
Venom Advertising, LLC
Effective date
2016-12-15
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:21:04

Label at a glance#

ProductSkinTek Skin Tag Remover
Active ingredientTHUJA OCCIDENTALIS LEAFY TWIG
Label structure7 sections

Dosage and administration

Apply to clean, dry skin. For best results, use at least twice daily for 6-8 weeks.

Label contents#

Full prescribing information#

Active ingredients:

OTC - ACTIVE INGREDIENT SECTION

Thuja Occidentalis 6X 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

Polypi, Naevi, Skin Tubercles Symptom Relief.

Indications:

INDICATIONS & USAGE SECTION

For the treatment of skin tags.

Warnings:

WARNINGS SECTION

  • For external use only.

If pregnant or breast feeding, 

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use.

Avoid contact with eyes. Rinse well if contact occurs

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact Poison Control Hotline immediately at 800-222-1222.

Directions:

DOSAGE & ADMINISTRATION SECTION

  • Apply to clean, dry skin.
  • For best results, use at least twice daily for 6-8 weeks.

Additional Information:

SPL UNCLASSIFIED SECTION

Store at room temperature. Do not use if temper evident seal is broken.

Inactive ingredients:

INACTIVE INGREDIENT SECTION

Helianthus annus (Sunflower) Oil, Melaleuca Alternifolia (Tree Leaf) Oil, Glycine Soja (Soybean) Oil, SD-Alcohol 40B, Prunus Amygdalus Dulcis (Sweet Almond) Oil, BHT

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2Label2

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71137-77171137-771-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
071b7f5c-230f-26bc-e063-6394a90a021643b7a5c0-b8f4-3270-e054-00144ff88e882023-10-07WarningsExact identifier
spl set id: 43b7a5c0-b8f4-3270-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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