Ratanhia Pellet
Product Images NDC 0220-4337

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Ratanhia (NDC 0220-4337). 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

2nd Panel

This Drug Facts panel details inactive ingredients including lactose and sucrose. It provides customer contact information for Boiron USA, including a phone number and email. Instructions on dispensing pellets are illustrated: turning the tube upside down, twisting the cap to dispense pellets into the cap, then carefully removing the cap to take pellets under the tongue. Manufacturer and distributor information for Boiron Inc. in Newtown Square, PA, is also shown.*

FDA Label Image

3rd Panel

A Drug Facts text panel for Ratanhia pellets containing Kramerlia Lappacea Root. It outlines the active ingredient amount per pellet, general uses, warnings to stop use and consult a doctor if symptoms persist beyond 3 days or worsen, and precautions for pregnant or breastfeeding individuals. Directions recommend dissolving 5 pellets under the tongue three times a day at symptom onset. Additional advice includes not using the product if the pellet dispenser seal is broken.*

FDA Label Image

Ratanhia8x

Ratanhia 8X homeopathic medicine pellets in an oral dosage form by Boiron. The label states it contains approximately 80 pellets. It is labeled for use related to hemorrhoids following constipation. Manufactured in France, with NDC 0220-4337-41. Includes lot and expiration date fields on the label.*

* 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.