Allium Cepa Pellet
Product Images NDC 15631-0015

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Allium Cepa (NDC 15631-0015). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rxhomeo Private Limited D.b.a. Rxhomeo, Inc, 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 Pellets Fda 15631 0015

Label Pellets Fda 15631 0015
This is a description of a homeopathic medicine containing Allium Cepa, Sucrose, and other ingredients listed using unreadable characters. The medicine is intended for the temporary relief of cough and cold symptoms. The dosage for adults is 4 to 6 pellets, to be taken orally three times a day. For children aged 2 and over, the dose is 12 pellets, which is equivalent to the adult dose. The medicine is not intended to treat severe medical conditions and should be used for self-treatment only. The product must be stored in a cool, dark place and kept out of reach of children. Adult women who are pregnant or breastfeeding should seek professional advice before taking this medicine. If symptoms persist for more than four days or worsen, discontinue use and seek help from a healthcare professional. The manufacturer is "Indradhanush" and the medicine contains 100 pellets. The text includes an NDC code, batch number, manufacturing and expiry date, but the actual numbers are unreadable.*
FDA Label Image

Mini Labels Pellets Fda15631 0015

Mini Labels Pellets Fda15631 0015
This is a description of Allium Cepa 1X, a remedy used for the temporary relief of cough and cold symptoms. The active ingredient is not specified. The remedy is taken orally, with adults advised to take 4 or 6 pellets, five times a day, or as directed by a physician. Children who are two years or older can take half the adult dose. Inactive ingredients include sucrose. The label is a mini size, and the product is packaged in blister packs. The NDC number is 15631-0015, and the batch was manufactured and has an expiry date that were not provided.*
FDA Label Image

Rxhomeo Secondary Packing Blister Pack

FDA Label Image

Rxhomeo Secondary Packing Carton Pack

Rxhomeo   Secondary Packing   Carton Pack
This is a product label for a lactose-free single homeopathic remedy manufactured in India according to the Homoeopathic Pharmacopoeia of the United States. The label contains warnings for its usage, storage, and the necessary actions in case of symptoms worsening, and if pregnant or nursing. The product has a US FDA Establishment number and distributed by Rehomeo, Inc. in Texas, USA. The label also contains notes related to the product's packing and distribution.*

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