Mancinella Pellet
Product Images NDC 0220-3283

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 Mancinella (NDC 0220-3283). 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

2nd Panel

2nd Panel
A drug facts panel continuing with inactive ingredients lactose and sucrose. It provides contact information for Boiron USA and distribution details. The panel includes illustrated instructions on how to dispense pellets from the product: turn tube upside down, twist until 5 pellets dispense into cap, then carefully remove cap to pour pellets under the tongue.*
FDA Label Image

3rd Panel

3rd Panel
Drug Facts panel featuring information about the active ingredient amount per pellet, uses referring to symptoms, warnings about stopping use and consulting a doctor if symptoms persist or in case of pregnancy or breastfeeding, directions for dosing pellets under the tongue, and additional information about not using the product if the pellet dispenser seal is broken.*
FDA Label Image

Mancin30c

Mancin30c
Label for Mancinella 30c pellets, a homeopathic medicine by Boiron, made in France. The label includes the product name, strength 30c, identification as a homeopathic medicine, lot and expiration fields, and a note about skin rash with oozing. It states approximately 80 pellets per container and advises peeling for drug facts and instructions. A disclaimer notes the product is 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.