Lycopodium Clavatum Pellet
Product Images NDC 76472-3024

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Lycopodium Clavatum (NDC 76472-3024). 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)

A 'Drug Facts' panel continuation for Lycopodium Clavatum 200ck pellets showing that the inactive ingredient is organic sucrose. It includes homeopathic dilution information and distributor contact details for SEVENE USA Inc. Illustrated instructions demonstrate how to dispense pellets by turning the tube upside down, twisting the cap, and using the cap to place pellets under the tongue. The bottom features a scenic background with the website ollois.com and the brand name 'Olloïs.'*

FDA Label Image

Page 1 (Label Ollois Lycopodium 200ck Page1)

Label for Olloïs Lycopodium Clavatum 200ck homeopathic medicine pellets. The label states it is organic and lactose-free, contains approximately 80 pellets weighing 4 grams, and is made in France. It includes a barcode, the NDC 76472-3024-1, and indicates traditional use for bloating, indigestion, and gas. The label also advises to pull for drug facts and directions for use.*

FDA Label Image

Page 2 (Label Ollois Lycopodium 200ck Page2)

Drug Facts panel for Lycopodium Clavatum 200CK sublingual pellets includes active ingredient, uses such as bloating, indigestion, and gas, warnings about use during pregnancy, overdose, and keeping out of reach of children, directions to dissolve 5 pellets under the tongue three times daily, and storage instructions to keep 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.