Silicea Pellet
Product Images NDC 76472-3034

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Silicea (NDC 76472-3034). 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)

Drug Facts panel for SILICEA 200ck pellets shows that the inactive ingredient is organic sucrose. It includes instructions with three steps on how to dispense pellets using a dispensing tube: turn the tube upside down, twist the cap to dispense pellets, and use the cap to place pellets under the tongue. Contact information for SEVENE USA and a website for more information are also provided.*

FDA Label Image

Page 1 (Label Ollois Silicea 200ck Page1)

The label for Silicea 200ck homeopathic medicine by Ollois shows this product as organic and lactose-free with an NDC of 76472-3034-1. It is indicated as approximately 80 pellets weighing 4 grams. The label highlights traditional use for constipation, fatigue, and irritability due to overwork. The product is made in France by SEVENE USA and comes as sublingual pellets.*

FDA Label Image

Page 2 (Label Ollois Silicea 200ck Page2)

Drug Facts panel for SILICEA 200CK pellets shows active ingredient Silicea 200CK, uses for constipation, fatigue, and irritability due to overwork. Includes warnings about stopping use if symptoms worsen, pregnancy and breastfeeding precautions, and keeping out of reach of children. Directions specify dissolving 5 pellets under the tongue three times daily until symptoms improve. Additional information advises storing at room temperature and not using if tamper seal is broken.*

* 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.