Thuja occidentalis 30C

Manufacturer
Boiron | Boiron, Inc.
Effective date
2025-11-21
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 02:35:21

Label at a glance#

ProductThuja occidentalis 30C
Active ingredientTHUJA OCCIDENTALIS LEAFY TWIG
Label structure12 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient** (in each pellet)

Thuja Occidentalis 30C HPUS (0.443)

The letters "HPUS" indicate that the component in this product are officially monographed in the Homeopathic Pharmacopoeia of the United States.

OTC - PURPOSE SECTION

Thuja Occidentalis 30C HPUS (0.443) ... For removal of common warts and plantar warts*

INDICATIONS & USAGE SECTION

Uses*

for removal of

  • common warts
  • plantar warts

OTC - ASK DOCTOR SECTION

Stop use and ask a doctor if the discomfort persists or wart becomes painful.

Stop use and ask a doctor if symptoms persist for more than 3 days or worsen.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of accidental overdose, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Adults and children: Dissolve 5 pellets under the tongue 2 times a day, mornings and evenings, until wart is removed or as directed by a doctor.

Adults and children: At the onset of symptoms, dissolve 5 pellets under the tongue 3 times a day until symptoms are relieved or as directed by a doctor.

OTC - DO NOT USE SECTION

Do not use if glued carton end flaps are open or if pellet dispenser seal is broken.

Do not use if pellet dispenser seal is broken.

INACTIVE INGREDIENT SECTION

lactose, sucrose

OTC - QUESTIONS SECTION

Boironusa.com

info@boiron.com

1-800-BOIRON-1

1-800-264-7661

Distributed by Boiron Inc.

Newtown Square, PA 19073

SPL UNCLASSIFIED SECTION

*CLAIMS BASED ON TRADITIONAL HOMEOPATHIC PRACTICE NOT ACCEPTED MEDICAL EVIDENCE. NOT FDA EVALUATED.
**C,K,CK, and X are homeopathic dilutions: see BoironUSA.com/info for details.

Turn tube upside down, twist until 5 pellets are dispensed, Remove cap and pour pellets under the tongue

3 Tubes, Approx. 80 Pellets Each, Total 240 Pellets, 16 Doses per tube

Pain-Free Wart Removal*

No Known Drug Interactions

Common Warts, Plantar Warts*

Wart Removal*

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel6897550689755030C30Cb2g1b2g130c30c

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0220-9356-432023-04-13C16284748780-1f386c649-ea73-0266-e053-dadaa90a7c1aThuja occidentalis 30C BONUS PACK
0220-9356-432023-01-30C16284748780-1f386c649-ea73-0266-e053-dadaa90a7c1aThuja occidentalis 30C BONUS PACK

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-9356-43Thuja occidentalis 30C30 [hp_C] in 1 PACKAGEPELLET305

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0220-93560220-9356-43

Ingredients#

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

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

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Thuja occidentalis 30CTHUJA OCCIDENTALISBoiron5e35616f-b057-0f18-e053-2991aa0a57492025-11-21Exact identifier
ndc (package): 0220-9356-43
ndc (product): 0220-9356
ndc11 (package): 00220935643
spl id: 441fe92c-ce78-3112-e063-6394a90a7c97
spl set id: 5e35616f-b057-0f18-e053-2991aa0a5749

Reported adverse events (FAERS/openFDA)#

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