Rhus Toxicodendron Pellet
Product Images NDC 76472-3031

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Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Rhus Toxicodendron (NDC 76472-3031). 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 Rhus Toxicodendron 200ck pellets includes the inactive ingredient organic sucrose, explains that C, K, CK, and X represent homeopathic dilutions, and provides distributor contact information for SEVENE USA. It also shows a three-step graphic instruction on how to dispense and use the sublingual pellets using the dispensing tube and cap, accompanied by branding and website information for Ollois.*
FDA Label Image

Page 1 (Label Ollois Rhus Tox 200ck Page1)

Page 1 (Label Ollois Rhus Tox 200ck Page1)
Label for Rhus Toxicodendron 200ck homeopathic medicine pellets by SEVENE USA. The green and pink label states the product name, strength 200ck, and identifies it as a lactose-free, organic homeopathy for all. It contains approximately 80 pellets weighing 4 grams. The label notes the product is made in France and includes the NDC 76472-3031-1 barcode.*
FDA Label Image

Page 2 (Label Ollois Rhus Tox 200ck Page2)

Page 2 (Label Ollois Rhus Tox 200ck Page2)
Drug Facts panel for Rhus Toxicodendron 200ck pellet showing active ingredient, uses for relief of cold sores and joint arthritis pain, warnings about use and overdose, directions to dissolve 5 pellets under the tongue three times daily, and storage instructions.*

* 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.