Walgreens Skin Tag Treatment

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Walgreens Skin Tag Treatment
Generic name: THUJA OCCIDENTALIS
Manufacturer: Walgreens
Product type: HUMAN OTC DRUG
SPL set ID: d9d76497-09b7-6979-e053-2a95a90a21fe
SPL ID: 09056983-cf95-4f82-e063-6294a90a858e
Version: 3
Effective date: 2023-10-31
Source export date: 2026-10-30
Source partition: 7
Source file: https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-30/0b630a6825fc0c8abba22d7c8fd4d069bde78bef928766047ddbb369119f337f/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run: 20261102T182004Z
Imported at: 2026-11-02 18:56:25

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 9 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Walgreens Skin Tag Treatment	openfda.brand_name
generic name		THUJA OCCIDENTALIS	openfda.generic_name
manufacturer name		Walgreens	openfda.manufacturer_name
ndc	package	0363-3100-10	openfda.package_ndc
ndc	product	0363-3100	openfda.product_ndc
ndc11	package	00363310010	derived:openfda.package_ndc
spl id		09056983-cf95-4f82-e063-6294a90a858e	id
spl set id		d9d76497-09b7-6979-e053-2a95a90a21fe	set_id
unii		1NT28V9397	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

For External use only . Avoid using near the eyes or mouth Keep out of the reach of children. In case of ingestion call Poison Control Center Hotline immediately at 1-800-222-1222 If pregnant or breast- feeding . Ask a health professional before use.

Reported adverse events (FAERS/openFDA)#

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