Arnica Montana Radix Pellet
Product Images NDC 0220-0518

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.

FDA Label Image

Label (2nd Panel)

This appears to be the label of a drug product, but the text is incomplete and contains typographical errors and non-English characters. The information is not sufficient to provide a useful description.*

FDA Label Image

Label (3rd Panel)

This is a description of a drug product. The active ingredient is not mentioned, but the product name is indicated on the front. The drug is in pellet form and each pellet contains 0.443 mg of the active ingredient. The symptoms that the drug is used for are listed on the front panel. The drug is not advised for pregnant or breastfeeding women without consulting a health professional. The suggested dosage is to dissolve 5 pellets under the tongue three times a day until symptoms are relieved or as directed by a doctor. It advises not to use if the pellet dispenser seal is broken and keep it out of the reach of children.*

FDA Label Image

Label (Arnmonrad30c 1st Image Only)

Arnica Montana is a homeopathic medicine used to relieve muscle pain, stiffness, swelling, and bruises resulting from injuries. This particular product contains approximately 80 pellets and is manufactured by OIRON in France. The lot number and expiration date are provided, and instructions for use can be found on the package.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.