SnoreStop® Anti-Snoring Chewable Tablets

split]] Our active ingredients draw from the power of plants, enhanced by minerals and other natural elements. This harmonious blend makes SnoreStop a safe, natural, and effective solution for conquering snoring. Ingredients & Purpose: Nux Vomica 4X HPUS: helps open constricted pharynx Belladonna 6X HPUS: helps decongest enlarged tonsils  Ephedra vulgaris* 6X HPUS: helps relieve congestion Hydrastis Canadensis 6X HPUS: helps decongest swollen tongue  Kali Bichromicum 6X HPUS: helps relieve stuffy nose  Teucrium marum 6X HPUS: helps open air passages  Histaminum hydrochloricum 12X HPUS: natural antihistamine  Dilution Scale: 6X is equal to one part per million. * Relax knowing that SnoreStop contains no ephedrine, pseudoephedrine, or alkaloids. Review our Certificate of Analysis for confirmation. Your peace of mind is paramount to us. With a proven safety record since 1995, SnoreStop is your trusted choice. The letters “HPUS” indicate that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of the United States. Chewable Tablets Certificate of Analysis Inactive ingredients: Anhydrous Lactose (3mg/tab), Croscamellose sodium, Dextrose (45 mg/tab), Lactose (180 mg/tab) Magnesium Stearate, Microcrystalline Cellulose. Lactose is a sugar from milk. Dextrose is a simple sugar (glucose). If you do not count lactose as a simple sugar then you only have 0.003 g of sugar per tablet. If you count lactose as sugar than you have 0.18 g of sugar per tablet (a minute amount). SnoreStop FastTabs is prepared in accordance with the Homeopathic Pharmacopoeia of the United States (HPUS). All ingredients are GRAS (generally recognized as safe) and are part of an official collection of accepted drug ingredients by the Federal Food, Drug and Cosmetic Act and are manufactured in FDA regulated laboratories in the USA. Each ingredient derives from plant, mineral or protein sources and is present only in harmless microscopic amounts in each dose. None of our ingredients contain any measurable amount of alkaloids, ephedrine or pseudo - ephedrine.  Dilution Scale: 6X is equal to one part per million. Claims follow requirement in CPG 400.400 and GLP of Sections 502 & 503 of the FDCA (“The Act”) and Part 201 Title 21 of the CFR to include Principle Display Panel of OTC Drug Labeling under 21 CFR 201.62. Uses and claims are taken from various authorized Materia Medica for references. They have not been reviewed by the Federal Drug Administration.