TERRASIL FAST AND NATURAL WART REMOVAL MAXIMUM STRENGTH- thuja occidentalis ointment

Drug Labeling and Warnings

Drug Details [pdf]

Active Ingredient

Thuja 3X HPUS

The letters HPUS indicate the component(s) in this product is (are) officially monographed in the Homeopathic Pharmacopeia of the United States.

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 ointment and cover with bandage as needed. Repeat procedure 2 times daily until skin improves. Store at room temperature. May stain fabrics.

Inactive Ingredients

beeswax (organic), bentonite (volcanic clay)**, cedarwood oil, cotton seed oil, jojoba seed oil, magnesium oxide, silver oxide, vegetable stearic acid (naturally sourced), zinc oxide.

** may contain this ingredient.

PRINCIPAL DISPLAY PANEL 

All Natural
terrasil®
FAST AND NATURAL WART REMOVAL OINTMENT
MAXIMUM STRENGTH
with Activated Minerals®

INGREDIENTS AND APPEARANCE

TERRASIL FAST AND NATURAL WART REMOVAL  MAXIMUM STRENGTH
thuja occidentalis ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 24909-186
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
THUJA OCCIDENTALIS WHOLE (UNII: 5HBV6WCE3N) (THUJA OCCIDENTALIS WHOLE - UNII:5HBV6WCE3N)	THUJA OCCIDENTALIS WHOLE	3 [hp_X]  in 1 g

Inactive Ingredients
Ingredient Name	Strength
BENTONITE (UNII: A3N5ZCN45C)
COTTONSEED OIL (UNII: H3E878020N)
JOJOBA OIL (UNII: 724GKU717M)
JUNIPERUS VIRGINIANA OIL (UNII: PAD4FN7P2G)
MAGNESIUM OXIDE (UNII: 3A3U0GI71G)
SILVER OXIDE (UNII: 897WUN6G6T)
STEARIC ACID (UNII: 4ELV7Z65AP)
WHITE WAX (UNII: 7G1J5DA97F)
ZINC OXIDE (UNII: SOI2LOH54Z)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 24909-186-50	50 g in 1 TUBE; Type 0: Not a Combination Product	01/01/2018
2	NDC: 24909-186-14	14 g in 1 TUBE; Type 0: Not a Combination Product	01/01/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		01/01/2018

Labeler - Aidance Skincare & Topical Solutions, LLC (018950611)

Establishment
Name	Address	ID/FEI	Business Operations
Aidance Skincare & Topical Solutions, LLC		018950611	manufacture(24909-186) , label(24909-186)