Arnica Montana Radix Pellet
Product Images NDC 0220-0518

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 Arnica Montana Radix (NDC 0220-0518). 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.

Product Images & Figures Index

FDA Label Image

Label (2nd Panel)

Label (2nd Panel)
A Drug Facts panel continuation showing inactive ingredients (lactose, sucrose), contact information for Boiron USA, and instructions for dispensing pellets in three steps: turn tube upside down, twist until 5 pellets dispense into the cap, then remove cap to place pellets under the tongue.*
FDA Label Image

Label (3rd Panel)

Label (3rd Panel)
A Drug Facts panel for Arnica montana radix pellets, listing the active ingredient quantity per pellet and directing users to the front panel for uses. It includes warnings to stop use if symptoms persist beyond 3 days and to consult a doctor if pregnant or breastfeeding. Directions recommend adults and children dissolve 5 pellets under the tongue three times daily until symptoms improve. Additional information advises against use if the pellet dispenser seal is broken.*
FDA Label Image

Label (Arnmonrad30c 1st Image Only)

Label (Arnmonrad30c 1st Image Only)
Label for Arnica montana radix 30C homeopathic medicine pellets by Boiron. The label states it contains approximately 80 pellets and is indicated for muscle pain, stiffness, swelling from injuries, and bruises. The product is made in France and includes lot and expiration date fields.*

* 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.