Active Ingredient:
HOMEOPATHIC DILUTION OF HPUS THUJA OCCIDENTALIS 30C.
Thuja Occidentalis Pellet
FDA Label NDC 76472-1167
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Sevene Usa for the product Thuja Occidentalis (NDC 76472-1167). 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 active ingredient:, traditionally use for:, directions:, otc - keep out of reach of children, otc - pregnancy or breast feeding, warnings:, other information:, use:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Traditionally Use For:
WARTS.
Directions:
(adults/children) Dissolve 5 pellets under the tongue 3 times a day until symptoms are relieved or as directed by a physician.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
Otc - Pregnancy Or Breast Feeding
If pregnant or breast-feeding, ask a health professional before use.
Warnings:
Stop use and ask a physician if symptoms persist for more than 3 days or worsen.
Other Information:
Store at room temperature.
Use:
Condition listed above or as directed by a physician.
Otc - Do Not Use
DO NOT USE IF PELLET DISPENSER SEAL IS BROKEN.
Inactive Ingredient:
Sucrose.
Questions?
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