Skin Tag Relief

Manufacturer
Quest Products, Inc. | Fill Tech USA
Effective date
2024-11-05
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
full-release
Hydrated at
2026-06-01 02:28:49

Label at a glance#

ProductSkin Tag Relief
Active ingredientTHUJA OCCIDENTALIS LEAFY TWIG
Label structure9 sections

Indications and uses

Symptomatic treatment of Skin Tags.

Dosage and administration

Apply 3 times daily to affected area. Skin tags will dry and flake away over several week period. Some individuals may be sensitive to essential oil. Skin test for tolerability. If irritation or reaction occurs, discontinue use.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Thuja Occidentalis 6X (HPUS) 1%

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

Cutaneous Skin Tags Relief

Uses

INDICATIONS & USAGE SECTION

Symptomatic treatment of Skin Tags.

Warnings

WARNINGS SECTION

For external use only.

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

OTC - WHEN USING SECTION

Avoid using near the eyes or mouth.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children. In case of ingestion call Poison Control Center hotline immediately at 1-800-222-1222.

OTC - DO NOT USE SECTION

Do not use if tamper evident seal is broken.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply 3 times daily to affected area. Skin tags will dry and flake away over several week period. Some individuals may be sensitive to essential oil. Skin test for tolerability. If irritation or reaction occurs, discontinue use.

Other ingredients

INACTIVE INGREDIENT SECTION

Cedar Leaf Oil, Melaleuca Alternifollia Leaf Oil (Tea Tree Oil), Ricinus Communis Seed Oil (Castor Oil).

SPL UNCLASSIFIED SECTION

There is no scientific evidence that this product works. The product's claims are based only on theories of homeopathy from the 1700's that are not acceptert by most modern medical experts.

PRINCIPAL DISPLAY PANEL - 10 mL Bottle Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

10mLPDP10mLPDP

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68229-100-022020-02-03C16284748780-19d75b9cf-fd88-f424-e053-dadaa90a57ceSkin Tag Relief
68229-100-022020-01-31C16284748780-19d75b9cf-fd88-f424-e053-dadaa90a57ceSkin Tag Relief

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68229-100-01Skin Tag Relief10 mL in 1 BOTTLE, WITH APPLICATOROIL107
68229-100-02Skin Tag Relief1 in 1 CARTONOIL17
68229-100-03Skin Tag Relief12.5 mL in 1 BOTTLE, WITH APPLICATOROIL12.57
68229-100-04Skin Tag Relief1 in 1 CARTONOIL17

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68229-100SKIN TAG RELIEF (THUJA OCCIDENTALIS LEAFY TWIG) OIL [QUEST PRODUCTS, INC.]7Current NDC, Legacy NDC, 4 package rows20241107_98fb9d4a-d0d2-425b-878b-927eebf53067.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
Thuja Occidentalis Leafy TwigACTIVE INGREDIENT1NT28V93971
Thuja Occidentalis Leafy TwigACTIVE MOIETY1NT28V93971
Castor OilINACTIVE INGREDIENTD5340Y2I9G1
Cedar Leaf OilINACTIVE INGREDIENTBJ169U4NLG1
Tea Tree OilINACTIVE INGREDIENTVIF565UC2G1

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
68229-10068229-100-01, 68229-100-02, 68229-100-03, 68229-100-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 10 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
Castor OilCASTOR OILD5340Y2I9GOINTMENT / TOPICAL14.9 %w/wExact identifier — unii+route
10 equally ranked IID candidates
Castor OilCASTOR OILD5340Y2I9GSOLUTION / TOPICAL1.38 %w/wExact identifier — unii+route
10 equally ranked IID candidates
Castor OilCASTOR OILD5340Y2I9GOINTMENT / TOPICAL14.9 %w/wExact identifier — unii+route
10 equally ranked IID candidates
Castor OilCASTOR OILD5340Y2I9GOINTMENT / TOPICAL14.9 %w/wExact identifier — unii+route
10 equally ranked IID candidates
Castor OilCASTOR OILD5340Y2I9GOINTMENT / TOPICAL14.9 %w/wExact identifier — unii+route
10 equally ranked IID candidates
Castor OilCASTOR OILD5340Y2I9GSOLUTION / TOPICAL1.38 %w/wExact identifier — unii+route
10 equally ranked IID candidates
Castor OilCASTOR OILD5340Y2I9GSOLUTION / TOPICAL1.38 %w/wExact identifier — unii+route
10 equally ranked IID candidates
Castor OilCASTOR OILD5340Y2I9GSOLUTION / TOPICAL1.38 %w/wExact identifier — unii+route
10 equally ranked IID candidates
Castor OilCASTOR OILD5340Y2I9GSOLUTION / TOPICAL1.38 %w/wExact identifier — unii+route
10 equally ranked IID candidates
Castor OilCASTOR OILD5340Y2I9GOINTMENT / TOPICAL14.9 %w/wExact identifier — unii+route
10 equally ranked IID candidates

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
Skin Tag ReliefTHUJA OCCIDENTALIS LEAFY TWIGQuest Products, Inc.98fb9d4a-d0d2-425b-878b-927eebf530672024-11-05WarningsExact identifier
ndc (package): 68229-100-01
ndc (package): 68229-100-02
ndc (package): 68229-100-04
ndc (package): 68229-100-03
ndc (product): 68229-100
ndc11 (package): 68229010002
ndc11 (package): 68229010003
ndc11 (package): 68229010001
ndc11 (package): 68229010004
spl id: 262e23fb-5ad8-bbde-e063-6394a90ab37b
spl set id: 98fb9d4a-d0d2-425b-878b-927eebf53067

Reported adverse events (FAERS/openFDA)#

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