THUJA OCCIDENTALIS- thuja occidentalis liquid
Washington Homeopathic Products

Disclaimer: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

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THUJA OCCIDENTALIS X

ACTIVE INGREDIENTS

THUJA OCCIDENTALIS

USES

To relieve the symptoms of warts.

KEEP OUT OF REACH OF CHILDREN

Keep this and all medicines out of reach of children.

INDICATIONS

Indications:

THUJA OCC Warts

STOP USE AND ASK DOCTOR

If symptoms persist/worsen or if pregnant/nursing, consult your practitioner.

DIRECTIONS

Adults: 4 drops into a tsp. of water 3 times a day. Children: 1/2 dose. Repeat at greater intervals as condition subsides. Or as directed bya lic. practitioner.

INACTIVE INGREDIENTS

Sucrose/Lactose

PRINCIPAL DISPLAY PANEL

The OTC potency range of THUJA OCC is 2x–30x, 1c–30c, 200c, 1m, 10m, 50m, and CM.

Label

Availability is subject to change.

All WHP single remedies are made to order; thus, the labels are printed on the same label stock, as the orders are filled.

‘Bottle Size,’ ‘Potency,’ and ‘Alcohol Percentage’ vary on the label depending on customer choice.

Standard bottle sizes for dilution-form remedies are 15ml, 30ml, 50ml, and 100ml.

THUJA OCCIDENTALIS
thuja occidentalis liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:71919-678
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (THUJA OCCIDENTALIS LEAFY TWIG - UNII:1NT28V9397)	THUJA OCCIDENTALIS LEAFY TWIG	30 [hp_C] in 1 mL

Ingredient Name	Strength
Inactive Ingredients
ALCOHOL (UNII: 3K9958V90M)
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:71919-678-07	15 mL in 1 VIAL, GLASS; Type 0: Not a Combination Product	05/17/2011
2	NDC:71919-678-08	30 mL in 1 VIAL, GLASS; Type 0: Not a Combination Product	05/17/2011
3	NDC:71919-678-09	50 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product	05/17/2011
4	NDC:71919-678-10	100 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product	05/17/2011

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		05/17/2011	03/24/2022

Labeler - Washington Homeopathic Products (084929389)

Name	Address	ID/FEI	Business Operations
Establishment
Washington Homeopathic Products		084929389	manufacture(71919-678)

Revised: 3/2022

Document Id: dafcd0d1-e031-1b60-e053-2a95a90a5b7d

Set id: 99c1ab11-4ed7-7bc2-e053-2a95a90a429e

Version: 2

Effective Time: 20220324

Washington Homeopathic Products