TERRASIL IPL RELIEF MAXIMUM STRENGTH- thuja occidentalis ointment

Drug Labeling and Warnings

Drug Details [pdf]

Active Ingredient

Thuja Occidentalis 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

Papule and Naevi Symptom Relief

Uses

Relief from symptoms of itch, papules (bumps) and lesions often associated with Molluscum per diagnosis and care by physician.

KEEP OUT OF REACH OF CHILDREN

Warnings

For external use only.
Virally based infections are contagious. This product will not stop the spread of Molluscum or other viruses.
Do not use - in the eyes - over large areas of the body - if you are allergic to any ingredient in this product.
Ask a doctor before use if pregnant or nursing.
Stop use and ask a doctor if condition worsens or symptoms persist for more than 7 days.

Directions

Wash and dry affected skin. Apply a thin layer of Terrasil 2-3 times daily. Store at room temperature.

Inactive Ingredients

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

PRINCIPAL DISPLAY PANEL - 14g Tube

All Natural
terrasil®
IPL RELIEF MAX

INGREDIENTS AND APPEARANCE

TERRASIL IPL RELIEF  MAXIMUM STRENGTH
thuja occidentalis ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 24909-147
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (THUJA OCCIDENTALIS LEAFY TWIG - UNII:1NT28V9397)	THUJA OCCIDENTALIS LEAFY TWIG	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)
PEPPERMINT OIL (UNII: AV092KU4JH)
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: 24909-147-14	14 g in 1 JAR; Type 0: Not a Combination Product	03/14/2014
2	NDC: 24909-147-44	44 g in 1 JAR; Type 0: Not a Combination Product	03/14/2014
3	NDC: 24909-147-15	14 g in 1 TUBE; Type 0: Not a Combination Product	12/29/2018
4	NDC: 24909-147-50	50 g in 1 TUBE; Type 0: Not a Combination Product	12/29/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		03/14/2014

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

Establishment
Name	Address	ID/FEI	Business Operations
Aidance Skincare & Topical Solutions, LLC		018950611	manufacture(24909-147) , label(24909-147)