SnoreStop FastTabs quick dissolving tablets target the mouth where soft tissue inflammation collapses on the airway preventing air from passing through.
'Designed to improve upper airway muscle tone, regulate nasal secretions as well as decreasing nasal allergic reactions.'- Dr. Derek Lipman, M.D. Author of 'Snoring from A to Zzzz'.
Chew one tablet 30 minutes before bedtime and repeat at bedtime. We recommend repeated use of the product for 3 to 5 consecutive nights. For Maximum Results, you can use it in conjunction with SnoreStop NasoSpray. Eat, drink, and/or take any medicine at least 30 minutes prior to taking SnoreStop at bedtime.
* Individual results may vary.
- Nux Vomica 4X: helps open constricted pharynx
- Belladonna 6X: helps decongest enlarged tonsils
- Ephedra vulgaris 6X: helps relieve congestion (there is no measureable amount of Ephedra or pseudoephedrine in our formula)
- Hydrastis Canadensis 6X: helps decongest swollen tongue
- Kali Bichromicum 6X: helps relieve stuffy nose
- Teucrium marum 6X: helps open air passages
- Histaminum hydrochloricum 12X: natural antihistamine
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 recognized as an official collection of accepted drug ingredients by the Federal Food, Drug and Cosmetic Act and are manufactured in FDA-approved laboratories. Each natural 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. SnoreStop is a natural homeopathic over-the-counter medicine regulated by the FDA.
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 and Administration.