Colchicum Autumnale Pellet
Product Images NDC 0220-1473

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 Colchicum Autumnale (NDC 0220-1473). 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 continues with inactive ingredients listed as lactose and sucrose. It provides contact information for questions or comments, including a phone number and website. There are illustrated instructions on how to dispense pellets, showing steps to turn the tube upside down, twist to dispense pellets into the cap, and carefully remove the cap to pour pellets under the tongue.*
FDA Label Image

Label (3rd Panel)

Label (3rd Panel)
Drug Facts panel text for Colchicum autumnale pellet, detailing the active ingredient amount per pellet, general uses, warnings about stopping use and consulting a doctor if symptoms persist, directions for dosing by adults and children, and other information such as not using the product if the pellet dispenser seal is broken.*
FDA Label Image

Label (Colaut1m)

Label (Colaut1m)
Label for Colchicum autumnale 1 m pellet, a homeopathic oral medication by Boiron. The label notes the product is made in France, includes approximately 80 pellets, and indicates the lot and expiration date fields. It is labeled for treatment of indigestion with nausea and sensitivity to odors and carries a disclaimer about homeopathic claims.*

* 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.