Staphysagria Pellet
Product Images NDC 76472-3036

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Staphysagria (NDC 76472-3036). 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)

This panel shows continued drug facts for STAPHYSAGRIA 200ck pellets, including the inactive ingredient organic sucrose and a note about homeopathic dilutions (C, K, CK, and X). It includes contact information for questions, distributor SEVENE USA, and step-by-step illustrated instructions for dispensing pellets from the tube. The bottom features branding text with a website link to ollois.com.*

FDA Label Image

Page 1 (Label Ollois Staphysagria 200ck Page1)

Label for Staphysagria 200ck homeopathic medicine pellets by SEVENE USA. The label indicates the product is organic, lactose-free, and made in France. It contains approximately 80 pellets weighing 4 grams total. The label includes the NDC 76472-3036-1 and suggests traditional use for minor cuts and surgical wounds.*

FDA Label Image

Page 2 (Label Ollois Staphysagria 200ck Page2)

Drug Facts panel for STAPHYSAGRIA 200ck pellet sublingual tablets. It lists the active ingredient as Staphysagria 200CK, intended uses for minor cuts and surgical wounds, and warnings such as stopping use if symptoms persist beyond 3 days, and keeping out of reach of children. Directions specify dissolving 5 pellets under the tongue three times daily. Additional information includes storage at room temperature and tamper-evidence seal 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.