Otc - Active Ingredient
THUJA OCCIDENTALIS 30C
WARTS
Thuja Occidentalis 30c Pellet
FDA Label NDC 0220-9356
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Boiron for the product Thuja Occidentalis 30c (NDC 0220-9356). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding otc - active ingredient, otc - purpose, indications & usage, warnings, otc - ask doctor, otc - pregnancy or breast feeding, otc - keep out of reach of children, dosage & administration, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
WART REMOVAL
Indications & Usage
FOR REMOVAL OF COMMON WARTS
Warnings
STOP USE AND ASK A DOCTOR IF WART BECOMES PAINFUL
Otc - Ask Doctor
STOP USE AND ASK DOCTOR IF WART BECOMES PAINFUL
Otc - Pregnancy Or Breast Feeding
IF PREGNANT OR BREAST FEEDING ASK A HEALTH PROFESSIONAL BEFORE USE
Otc - Keep Out Of Reach Of Children
KEEP OUT OF REACH OF CHILDREN
Dosage & Administration
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
Otc - Do Not Use
DO NOT USE IF PELLET DISPENSER SEAL IS BROKEN
Inactive Ingredient
LACTOSE, SUCROSE
Otc - Questions
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