SnoreStop for Pets Anti-Snoring Spray

split]] Our gentle snore relief medicine is powered by plants using GRAS (generally recognized as safe) FDA-approved natural ingredients. SnoreStop for Pets spray is a water based solution.   ‘4X’ and ‘6X’, '12X' the potency of the active ingredient is indicated by the number and letter combination listed next to the ingredient. The higher the number the higher the potency. But even our highest potency (12X) result in only trace amounts of the active ingredients used in the medicine, thus ensuring a high margin of safety.  To be accepted as a homeopathic medicine by the FDA, our product must contain ingredients that are identified in the Homeopathic Pharmacopoeia of the United States (HPUS) or that are accepted as homeopathic under the principles of homeopathy. Active Ingredients & Purpose: Nux Vomica 4X, 6X 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 12X HPUS: natural antihistamine  *SnoreStop does not contain ephedrine or pseudoephedrine, or alkaloids of any kind.  SnoreStop for Pets spray is prepared in accordance with the Homeopathic Pharmacopoeia of the United States (HPUS). All ingredients are recognized as an official collection of accepted drug ingredients by the Federal Food, Drug and Cosmetic Act and are manufactured in FDA-approved laboratories in the USA. Each ingredient comes either from plant, mineral or protein sources and is present only in harmless microscopic amounts in each dose. None of our ingredients contain any 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.