FDA.reportPublic FDA data

Walgreens Skin Tag Treatment

Manufacturer
Walgreens
Effective date
2023-10-31
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:22:59

Label at a glance#

ProductWalgreens Skin Tag Treatment
Active ingredientTHUJA OCCIDENTALIS LEAFY TWIG
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Thuja Occidentalis 6X (HPUS)

OTC - PURPOSE SECTION

Cutaneous Skin Tags Aid

INDICATIONS & USAGE SECTION

Helps with symptomatic treatment of Skin Tags

WARNINGS SECTION

For External use only. 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 - PREGNANCY OR BREAST FEEDING SECTION

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

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 SAFETY INFORMATION

Do not use if cap tamper evident seal is broken or miss

INACTIVE INGREDIENT SECTION

Cedar Leaf Oil, Melaleuca Alternifollia leaf Oil, Ricinus Communis Seed Oil.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package CartonPackage CartonPackage LabelPackage Label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0363-3100-10Walgreens Skin Tag Treatment10 mL in 1 BOTTLE, GLASSLIQUID103

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0363-3100WALGREENS SKIN TAG TREATMENT (THUJA OCCIDENTALIS) LIQUID [WALGREENS]3Current NDC, 1 package rows20231102_d9d76497-09b7-6979-e053-2a95a90a21fe.zip

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
0363-31000363-3100-10

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
TEA TREE OILVIF565UC2GIACT
THUJA OCCIDENTALIS LEAFY TWIG1NT28V9397ACTIB
CASTOR OILD5340Y2I9GIACT
CEDAR LEAF OILBJ169U4NLGIACT

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
Walgreens Skin Tag TreatmentTHUJA OCCIDENTALISWalgreensd9d76497-09b7-6979-e053-2a95a90a21fe2023-10-31WarningsExact identifier
ndc (package): 0363-3100-10
ndc (product): 0363-3100
ndc11 (package): 00363310010
spl id: 09056983-cf95-4f82-e063-6294a90a858e
spl set id: d9d76497-09b7-6979-e053-2a95a90a21fe

Reported adverse events (FAERS/openFDA)#

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