Kali Arsenicosum Pellet
Product Images NDC 0220-2847

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Kali Arsenicosum (NDC 0220-2847). 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)

Partial Drug Facts panel for Kali arsenicosum (potassium arsenite anhydrous) pellets. Lists inactive ingredients lactose and sucrose, contact information for Boiron USA, and homeopathic dilutions instructions. Includes illustrated directions on dispensing pellets from the container: turn tube upside down, twist to dispense five pellets into cap, then remove cap carefully to place pellets under the tongue.*

FDA Label Image

Label (3rd Panel)

Drug Facts panel for Kali arsenicosum pellet oral medication. It includes sections on the active ingredient amount per pellet, uses referencing the front panel symptoms, warnings to stop use and consult a doctor if symptoms worsen or persist, and caution for pregnant or breastfeeding individuals. Directions advise dosing 5 pellets under the tongue three times daily until symptoms improve. Additional information notes not using if the pellet dispenser seal is broken.*

FDA Label Image

Label (Kalars200ck)

Kali arsenicosum 200 ck homeopathic medicine pellet label by Boiron, made in France. The label includes a lot and expiration date section, states approximately 80 pellets per container, and mentions use for dry skin rash with itching. It notes that claims are based on traditional homeopathic practice and not evaluated by the FDA.*

* 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.