Abies Nigra Pellet
Product Images NDC 0220-0011

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 Abies Nigra (NDC 0220-0011). 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 continuation lists inactive ingredients lactose and sucrose, contact information for Boiron USA including email and phone number, and a distribution address in Newtown Square, PA. Instructions are given for dispensing oral pellets in three steps with illustrations: turning the tube upside down, twisting until 5 pellets fall into the cap, then removing the cap to place pellets under the tongue.*
FDA Label Image

Label (3rd Panel)

Label (3rd Panel)
A Drug Facts panel for Abies Nigra pellet oral medication. It lists active ingredient amount per pellet, usage guidance to see front panel symptoms, warnings about prolonged use and pregnancy, directions to dissolve 5 pellets under the tongue three times daily, and other information including not using if pellet dispenser seal is broken.*
FDA Label Image

Label (Abinig30c)

Label (Abinig30c)
Label of Abies Nigra 30C oral pellets by Boiron, a homeopathic medicine made in France. The label includes warnings that claims are based on traditional homeopathic practice and not accepted medical evidence. It lists symptoms such as acid indigestion, sour stomach, and heartburn, and contains approximately 80 pellets per container.*

* 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.