Active Ingredient
Thuja Occidentalis
The letters HPUS indicate the component(s) in this product is (are) officially monographed in the Homeopathic Pharmacopeia of the United States
Terrasil Wart Treatment
FDA Label NDC 24909-113
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Aidance Skincare & Topical Solutions, Llc for the product Terrasil Wart Treatment (NDC 24909-113). 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, keep out of reach of children., directions, inactive ingredients, principal display panel - 44g label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Wart Symptom Relief
Uses
For the treatment of warts
Warnings
For external use only.
Ask a doctor before use if pregnant or nursing.
When using this product, do not get into eyes.
Keep Out Of Reach Of Children.
If swallowed, call poison control or seek medical help.
Directions
Wash and dry affected skin. Apply a thin layer of Terrasil. Repeat procedure 2-3 times daily until skin improves. Warts will dry and flake away over 3 to 6 week period. Store at room temperature.
Inactive Ingredients
cera alba (organic beeswax), juniperus virginiana (cedarwood) oil, silver oxide, magnesium oxide, simmondsia chinensis (jojoba) seed oil, zinc oxide
Principal Display Panel - 44G Label
terrasil
Wart TreatmentFast - Painless - All-Natural
Jar Label (Terrasil Wart Homeo Reg Label 44g 101612v1.7)
* Please review the disclaimer below.
