Otc - Active Ingredient
Thuja Occidentalis 6X (HPUS)
Walgreens Skin Tag Treatment Liquid
FDA Label NDC 0363-3100
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Walgreens for the product Walgreens Skin Tag Treatment (NDC 0363-3100). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding otc - active ingredient, otc - purpose, indications & usage, warnings, otc - keep out of reach of children, otc - pregnancy or breast feeding, dosage & administration, other safety information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Cutaneous Skin Tags Aid
Indications & Usage
Helps with symptomatic treatment of Skin Tags
Warnings
For External use only. Avoid using near the eyes or mouth
Otc - Keep Out Of Reach Of Children
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
If pregnant or breast- feeding. Ask a health professional before use.
Dosage & 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.
Other Safety Information
Do not use if cap tamper evident seal is broken or miss
Inactive Ingredient
Cedar Leaf Oil, Melaleuca Alternifollia leaf Oil, Ricinus Communis Seed Oil.
Package Label.Principal Display Panel
Package Label (24 1109 Lo)
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