Spigelia Anthelmia
Product Images NDC 15631-0409

This is a description of a homeopathic medication called Spigelia Anthelmia. The ingredients include Sucrose and the active ingredient, which is not visible in the text. The medication is used for temporary relief of nasal congestion, but it is not FDA approved. The recommended dosage is 4 to 6 pellets taken orally three times a day for adults and 12 pellets for children age two and older. This medication is for self-limiting conditions and should be discontinued if symptoms do not improve or worsen after four days. Pregnant or breastfeeding women should seek professional advice before using this medication. The medication should be kept out of reach of children, stored in a cool, dark place, and not used if the capsule is broken or missing. The text also includes the address of the manufacturer and the product's NDC code.*

This is a medication for temporary relief of nasal congestion. The active ingredient has not been mentioned, but the inactive ingredient is Sucrose. It is a homeopathic medicine not approved by the FDA. The medication comes in pellets and should be taken orally. Dosage for adults is four pellets, three times per day or as directed by a physician. Children over two years old should take half the adult dose. The medication comes in blister packs with specific pack sizes and has a unique identifier number: NDC15631-0409. The manufacturing date and expiration date have been obscured.*

This is a label for a single homeopathic remedy manufactured according to the Homeopathic Pharmacopoeia of the United States (HPUS). The product is lactose-free and distributed by Rehomeo, Inc. The label provides warnings against using the product for serious conditions, advises seeking medical advice if symptoms persist, and cautions pregnant or nursing women against using it. It also instructs users to keep the medication out of reach of children, store it in a cool, dark place, and not to use it if the seal is broken or missing. The product is manufactured by Rihomeo Prvate Limted in India, and the label gives a US FDA establishment number. The notes related to packing indicate that the product may be packaged in a bottle, container or blister pack, depending on size.*