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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DRUG FACTS

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 TypeHUMAN OTC DRUGItem Code (Source)NDC:71919-678
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (THUJA OCCIDENTALIS LEAFY TWIG - UNII:1NT28V9397) THUJA OCCIDENTALIS LEAFY TWIG30 [hp_C]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71919-678-0715 mL in 1 VIAL, GLASS; Type 0: Not a Combination Product05/17/2011
2NDC:71919-678-0830 mL in 1 VIAL, GLASS; Type 0: Not a Combination Product05/17/2011
3NDC:71919-678-0950 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product05/17/2011
4NDC:71919-678-10100 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product05/17/2011
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic05/17/2011
Labeler - Washington Homeopathic Products (084929389)
Establishment
NameAddressID/FEIBusiness Operations
Washington Homeopathic Products084929389manufacture(71919-678)

Revised: 7/2019
Document Id: 99c1ab11-4ed8-7bc2-e053-2a95a90a429e
Set id: 99c1ab11-4ed7-7bc2-e053-2a95a90a429e
Version: 1
Effective Time: 20190715
 
Washington Homeopathic Products