Mancinella Pellet
Product Images NDC 0220-3283

View Photos of 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.

FDA Label Image

2nd Panel

2nd Panel
This is the packaging information for a drug, but the name of the drug is not available. It provides details about inactive ingredients and a website and helpline for further information. The text also mentions the homeopathic dilutions G, K, CK, and X, and directs readers to visit the website for more information on these. There is also a string of unreadable characters at the end of the text.*
FDA Label Image

3rd Panel

3rd Panel
This is a drug information label. The label contains information on the active ingredient, uses, warnings, and directions of use for a drug. The drug contains 0.443 mg of the active ingredient per pellet. The user is advised to seek medical attention if symptoms persist for more than 3 days, or if they worsen after taking the drug. The drug is not recommended for pregnant or breastfeeding women, and it is advised to consult a healthcare professional before use. The user is advised to keep the drug out of reach of children. The drug should be dissolved under the tongue three times a day or as directed by a doctor. This information is not complete, and more details may be found on the label.*
FDA Label Image

Mancin30c

Mancin30c
This is a homeopathic medicine called Mancinella 30ยข, manufactured in France. The package contains about 80 pills and is labeled to provide drug facts and instructions for use. The specific condition it targets is "skin rash with oozing". The product is registered under the Homeopathic Pharmacopoeia of the United States (HPUS) with the NDC code 0220-3283-41. The lot expiration date is not provided.*

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