Arsenicum Sulphuratum Rubrum Pellet
Product Images NDC 0220-0548

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Arsenicum Sulphuratum Rubrum (NDC 0220-0548). 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 partial Drug Facts panel for Arsenicum sulphuratum rubrum pellets lists inactive ingredients including lactose and sucrose. It provides contact information for Boiron USA and instructions for use, with illustrations showing how to dispense pellets from the container by turning it upside down, twisting to dispense pellets into the cap, and pouring them under the tongue.*

FDA Label Image

Label (3rd Panel)

A Drug Facts panel for Arsenicum sulphuratum rubrum oral pellets. It lists the active ingredient amount per pellet, general uses referring to symptom relief, warnings about use duration and pregnancy or breastfeeding, directions for dosing under the tongue, and a note on pellet dispenser seal integrity.*

FDA Label Image

Label (Arssulrub30c)

Label for Arsenicum sulphuratum rubrum 30C pellets, a homeopathic oral pellet medicine manufactured by Boiron in France. The label includes the HPUS NDC 0220-0548-41, mentions the product is for dry cough with hypersensitivity to cold, and states it contains approximately 80 pellets. It also includes a disclaimer about claims based on traditional homeopathic practice, not accepted medical evidence or FDA evaluation.*

* 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.