Thuja Occidentalis Pellet
Product Images NDC 76472-3039

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Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Thuja Occidentalis (NDC 76472-3039). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sevene Usa, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Page 3 (Page3 Label Ollois Common)

Page 3 (Page3 Label Ollois Common)
This Drug Facts panel for THUJA OCCIDENTALIS 200ck pellet includes the inactive ingredient organic sucrose. It explains that C, K, CK, and X denote homeopathic dilutions and provides distributor contact information for SEVENE USA Inc. The panel features instructions on how to dispense pellets by turning the tube upside down and twisting the cap to dispense, then using the cap to place pellets under the tongue. The bottom includes a promotional message and website for Ollois.*
FDA Label Image

Page 1 (Label Ollois Thuja 200ck Page1)

Page 1 (Label Ollois Thuja 200ck Page1)
Label for Thuja Occidentalis 200ck homeopathic medicine pellets by SEVENE USA. The label states it is organic, lactose-free, and traditionally used for warts. Contains approximately 80 pellets weighing 4g. The product is made in France. The NDC 76472-3039-1 and a barcode are visible. The dosage form is sublingual pellets.*
FDA Label Image

Page 2 (Label Ollois Thuja 200ck Page2)

Page 2 (Label Ollois Thuja 200ck Page2)
Drug Facts panel for THUJA OCCIDENTALIS 200CK pellet includes active ingredient, uses (warts), warnings for pregnancy, overdose, and keeping out of reach of children, directions to dissolve 5 pellets under the tongue 3 times daily, and storage instructions at room temperature.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.