Active Ingredient
THUJUS OFFICINALIS 6X
Skin Tag Solution
FDA Label NDC 69368-2454
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Vitacost.com, Inc. for the product Skin Tag Solution (NDC 69368-2454). 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 active ingredient, purpose, uses, warnings, directions, other information, package label.principal display panel, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
POLPI, NAEVI, SKIN TUBERCLES SYMPTOMS
Uses
SYMPTOMATIC TREATMENT OF SKIN TAGS
Warnings
FOR EXTERNAL USE ONLY. AVOID USING NEAR EYES.
IF PREGNANT OR BREAST FEEDING, ASK A MEDICAL PROFESSIONAL.
Directions
- APPLY 3-4 TIMES DAILY TO AFFECTED AREA.
- SKIN TAGS WILL DRY AND FALL OFF OVER A 4 TO 8 WEEK PERIOD WITH REGULAR USE.
- IF IRRITATION OCCURS, DISCONTINUE USE.
Other Information
- PROTECT THIS PRODUCT FROM EXCESSIVE HEAT AND DIRECT SUNLIGHT.
Inactive Ingredients
BHT, GLYCINE SOYA (SOYBEAN) OIL, HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL, MELALEUCA ALTERNIFOLIA (TEA TREE) OIL, PRUNUS AMYGDALUS DULCIS (SWEET ALMOND) OIL AND SD-ALCOHOL 40B.
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