Naja Tripudians Pellet
Product Images NDC 0220-3544

3 FDA label images from Boiron · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Naja Tripudians (NDC 0220-3544). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Boiron, 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

Label (2nd Panel)

Label (2nd Panel)
This Drug Facts panel for Naja tripudians pellets includes inactive ingredients lactose and sucrose, contact information for Boiron USA, and instructions for homeopathic dilutions. It also provides a step-by-step guide for dispensing pellets: turning the tube upside down, twisting to dispense 5 pellets into the cap, and carefully removing the cap to place pellets under the tongue.*
FDA Label Image

Label (3rd Panel)

Label (3rd Panel)
Drug Facts panel for Naja tripudians pellets containing 0.443 mg of the active ingredient per pellet. It includes information on uses, warnings to stop use if symptoms worsen or persist beyond three days, and advice for pregnant or breastfeeding users. Directions for dosing are listed, as well as a note not to use if the pellet dispenser seal is broken.*
FDA Label Image

Label (Najtri1m)

Label (Najtri1m)
Naja tripudians 1 m pellet oral homeopathic medicine bottle label by Boiron. The label states it is made in France and contains approximately 80 pellets. The label includes a lot and expiration date section and a note to peel for drug facts and instructions for use. It also contains a disclaimer about traditional homeopathic practice claims not accepted by the FDA.*

* 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.