Colchicum Autumnale Pellet
Product Images NDC 15631-0150

This is a description for a homeopathic medicine called "Colchicum Autumnale 3X Eike" that comes in the form of pellets. The active ingredient is not specified, but the inactive ingredients are listed as sucrose. This medicine is to be taken orally, with adults advised to take 4 to 6 pellets three times a day, while children over two years old should take 12 pellets, which is equivalent to the adult dose. It is indicated to provide temporary relief for numbness of fingertips. The product is not evaluated by the FDA and should only be used for self-limiting conditions. Pregnant or nursing women are advised to consult a healthcare professional before taking this product. The medication should be kept out of reach of children, and the container should be closed tightly after use. The label specifies the manufacturer and location, the expiration date, as well as a batch number and National Drug Code.*

This is a label of a medication that uses an active ingredient called Colchicum Autumnale 3X and an inactive ingredient called Sucrose. It is intended for temporary relief of numbness of finger lips. The recommended dosage for adults is to take 4 or pellets by mouth, three times daily, or as directed by a physician. Children 2 years and older can take 1/2 the adult dose. The medication is not approved by the FDA, and the label includes a disclaimer that it is based on irrational homeopathic principles and not accepted medical evidence. The label also includes information on the product's batch number, manufacturing date, and expiration date.*

This is a description of a homeopathic medicine with a lactose-free formulation that's packaged according to the Homoeopathic Pharmacopoeia of the United States. It's a single homeopathic remedy that comes with a warning against using it for serious conditions and possible interactions if pregnant or nursing. The product is distributed by Rehomeo, Inc from Texas, USA and manufactured by Rihomeo Private Limited from Hyderabad, India. There are notes on the packaging and labeling of the medicine, including that the manufacturer US FDA Establishment number is always printed.*