THUJA- thuja occidentalis leafy twig liquid

Thuja by

Drug Labeling and Warnings

Thuja by is a Homeopathic medication manufactured, distributed, or labeled by PEKANA Naturheilmittel GmbH, PEKANA GmbH. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Indications

For skin tags and warts. Application of this homeopathic remedy for the designated usage is exclusively based on homeopathic experience. With severe forms of this disease, a clinically proven therapy is indicated.

Dosage

Unless otherwise prescribed, adults take 15-20 drops, 3 times per day. For pediatric dosages, consult your practitioner.

Warning

If symptoms persist, contact a licensed practitioner. If you have known sensitivity to any of the ingredients, please consult your licensed practitioner before use. If you are pregnant or nursing a baby, seek the advice of a health care professional before use.

Keep out of the reach of children.

Protect from light and heat.

Tamper Evident

Do not use this product if tamper evident strip is broken or removed from base of cap.

Ingredients

• Thuja occidentalis: 3X

INACTIVE INGREDIENT

Contains 69% alcohol by volume.

QUESTIONS

To report adverse events, contact BioResource at 321B Blodgett Street, Cotati, CA 94931

SPL UNCLASSIFIED SECTION

Manufactured by:
PEKANA® GmbH
D-88353 Kisslegg

Distributed by: BioResource Inc.
Cotati, CA 94931

PRINCIPAL DISPLAY PANEL - 50 ml Bottle Box

THUJA™
Oral Drops

Homeopathic Medicine

For skin tags and warts

1.7 FL OZ
(50 ml)

PEKANA®

INGREDIENTS AND APPEARANCE

THUJA 
thuja occidentalis leafy twig liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 59469-157
Route of Administration	ORAL

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 50 mL

Inactive Ingredients
Ingredient Name	Strength
Alcohol (UNII: 3K9958V90M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59469-157-10	1 in 1 BOX	05/01/2005
1		50 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
UNAPPROVED HOMEOPATHIC		05/01/2005

Labeler - PEKANA Naturheilmittel GmbH (320344542)

Establishment
Name	Address	ID/FEI	Business Operations
PEKANA GmbH		320344542	MANUFACTURE(59469-157)