Sepia Pellet
Product Images NDC 76472-3033

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Sepia (NDC 76472-3033). 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 contains the continued Drug Facts for SEPIA 200ck pellets, listing organic sucrose as the inactive ingredient and explaining homeopathic dilutions (C, K, CK, X). It includes the distributor SEVENE USA's contact information, an email address, and a toll-free number. Illustrated dispensing instructions show how to turn the tube upside down, twist the cap to dispense pellets, and use the cap to place pellets under the tongue. The panel also features a slogan and website for the brand Ollois.*

FDA Label Image

Page 1 (Label Ollois Sepia 200ck Page1)

Label for SEPIA 200ck homeopathic pellets by SEVENE USA, NDC 76472-3033-1. The sublingual pellets are traditionally used for menstrual symptoms and moodiness. The label notes the product is organic and lactose-free, contains approximately 80 pellets totaling 4 grams, and is made in France.*

FDA Label Image

Page 2 (Label Ollois Sepia 200ck Page2)

Drug Facts panel for SEPIA 200CK pellets describing active ingredient as Sepia 200CK, uses for menstrual symptoms and moodiness, warnings about stopping use if symptoms persist, pregnancy precautions, keeping out of reach of children, overdose advice, directions to dissolve 5 pellets under the tongue 3 times daily, storage instructions at room temperature, tamper-evidence note, and organic verification by Alpes Contrôle.*

* 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.