Causticum Pellet
Product Images NDC 15631-0118

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 Causticum (NDC 15631-0118). 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 0118

Label Pellets Fda 15631 0118
This is a description for a homeopathic medicine called "CAUSTICUM 2X EikE" available in pellet form. The medicine is meant for providing temporary relief from cough symptoms. The recommended dose for adults is 4 to 6 pellets thrice a day or as advised by a health professional. Children over 2 years of age can take 12 pellets per dose, which is equal to the adult dosage. This medicine contains active and inactive ingredients like sucrose. It is important to consult with a health professional before using this product if pregnant or nursing. The medicine should be stored in a cool and dark place, out of reach from children. Manufacturing and expiration dates are mentioned on the product. NDC number is also provided on the product along with address and contact information of the manufacturer.*
FDA Label Image

Mini Labels Pellets Fda15631 0118

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 description for a single homeopathic remedy that is lactose-free, according to the Homoeopathic Pharmacopoeia of the United States (HPUS). The product is manufactured by Rehomeo, Inc and distributed from Texas, USA. The product packaging and labelling depend on the pack size/contents, and the manufacturer's US FDA Establishment number is always printed. The product should not be used if symptoms do not improve in four days, or worsen; and if pregnant or nursing, one should seek professional advice before taking it.*

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