Argentum Nitricum Pellet
Product Images NDC 76472-3003

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Argentum Nitricum (NDC 76472-3003). 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

Page3_label_ollois_common (Page3 Label Ollois Common)

Continued Drug Facts panel for Argentum Nitricum 200ck pellets showing the inactive ingredient as organic sucrose. Includes homeopathic dilution notes, distributor contact information (SEVENE USA), and customer support email and phone number. Provides illustrated instructions on dispensing pellets by turning the tube upside down, twisting the cap, and placing pellets under the tongue. Features branding with 'Welcome to our playground' and Olloïs logo and website.*

FDA Label Image

Label_ollois_argentum_200ck_page1 (Label Ollois Argentum 200ck Page1)

Label for Argentum Nitricum 200ck homeopathic medicine pellets by SEVENE USA, NDC 76472-3003-1. The sublingual pellets are organic and lactose-free, with approximately 80 pellets in a 4g package. The label notes traditional use for nervous anticipation with occasional heartburn and stage fright. Made in France.*

FDA Label Image

Label_ollois_argentum_200ck_page2 (Label Ollois Argentum 200ck Page2)

Drug Facts panel for Argentum Nitricum 200ck pellets with active ingredient Argentum Nitricum 200CK. It includes uses for nervous anticipation and occasional heartburn, warnings about pregnancy, breastfeeding, overdose, and keeping out of reach of children, directions to dissolve 5 pellets under the tongue three times a day, and storage instructions 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.