Label at a glance#

ProductThuja Occidentalis

Active ingredientTHUJA OCCIDENTALIS LEAFY TWIG

Label structure8 sections

Indications and uses

To relieve the symptoms of warts.

Dosage and administration

Adults: Dissolve 3 to 5 under the tongue three times a day or as directed by Lic. Practitioner. Take at greater intervals as condition subsides. Children: Dissolve 3 to 5 under the tongue three times a day or as directed by Lic. Practitioner. Take at greater intervals as condition subsides.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

THUJA OCC

USES

OTC - PURPOSE SECTION

To relieve the symptoms of warts.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep this and all medicines out of reach of children.

INDICATIONS

INDICATIONS & USAGE SECTION

Indications:

THUJA OCC Warts

STOP USE AND ASK DOCTOR

WARNINGS SECTION

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

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Adults: Dissolve 3 to 5 under the tongue three times a day or as directed by Lic. Practitioner. Take at greater intervals as condition subsides. Children: Dissolve 3 to 5 under the tongue three times a day or as directed by Lic. Practitioner. Take at greater intervals as condition subsides.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Sucrose/Lactose

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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

Availability is subject to change.

Thuja2023

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’ and ‘Potency’ vary on the label depending on customer choice.

Standard bottle sizes for pellet-form remedies are 2 dram, 4 dram, 1 ounce, 2 ounce, and 4 ounce.

here

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
68428-677-03	2025-01-30	C162847	48780-1	2cef2736-a6fb-d83d-e063-dadaa90ab31f	DRUG FACTS
68428-677-05	2025-01-30	C162847	48780-1	2cef2736-a6fb-d83d-e063-dadaa90ab31f	DRUG FACTS
68428-677-06	2025-01-30	C162847	48780-1	2cef2736-a6fb-d83d-e063-dadaa90ab31f	DRUG FACTS
68428-677-11	2025-01-30	C162847	48780-1	2cef2736-a6fb-d83d-e063-dadaa90ab31f	DRUG FACTS
68428-677-12	2025-01-30	C162847	48780-1	2cef2736-a6fb-d83d-e063-dadaa90ab31f	DRUG FACTS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
68428-677-03	Thuja Occidentalis	75 in 1 VIAL, GLASS	PELLET	75	3
68428-677-05	Thuja Occidentalis	150 in 1 VIAL, GLASS	PELLET	150	3
68428-677-06	Thuja Occidentalis	1200 in 1 BOTTLE, GLASS	PELLET	1200	3
68428-677-11	Thuja Occidentalis	300 in 1 BOTTLE, GLASS	PELLET	300	3
68428-677-12	Thuja Occidentalis	600 in 1 BOTTLE, GLASS	PELLET	600	3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
68428-677	THUJA OCCIDENTALIS (THUJA OCCIDENTALIS LEAFY TWIG) PELLET [WASHINGTON HOMEOPATHIC PRODUCTS]	3	Legacy NDC, 5 package rows	20231021_54a3a414-15dd-4c67-ab72-4f3e8b38841b.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 4 matching rows.

Thuja Occidentalis
THUJA OCCIDENTALIS LEAFY TWIG
SUCROSE
LACTOSE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
68428-677	68428-677-03, 68428-677-05, 68428-677-11, 68428-677-12, 68428-677-06

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
SUCROSE	C151H8M554	IACT
LACTOSE	J2B2A4N98G	IACT
THUJA OCCIDENTALIS LEAFY TWIG	1NT28V9397	ACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
08285f08-aeba-7a19-e063-6294a90a1810			54a3a414-15dd-4c67-ab72-4f3e8b38841b	2023-10-20	Warnings	Exact identifier spl id: 08285f08-aeba-7a19-e063-6294a90a1810 spl set id: 54a3a414-15dd-4c67-ab72-4f3e8b38841b

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.