SnoreStop Anti-Snoring Throat Spray

SnoreStop Throat Spray: The Natural Solution for Throat-Based Snoring

Breathe freely and sleep soundly with SnoreStop Throat Spray, a fast-acting, natural remedy designed to reduce throat-based snoring. Trusted since 2001, this oil-free spray is easy to use and works to improve your sleep quality by opening airways and reducing inflammation.

Key Features:

• Targets Throat-Based Snoring: Helps alleviate inflammation and irritation in the throat to ensure better airflow.
• Natural Ingredients: Safe, non-addictive, and free from known side effects.
• Easy to Use: A quick spray under the tongue and in the back of the throat at bedtime sets you up for a peaceful night’s rest.
• Proven Effectiveness: SnoreStop is the only medically proven, over-the-counter snoring solution that is not a device.
• Trusted Quality: FDA-regulated, GMP-certified, and proudly made in the USA.

Why Choose SnoreStop?

Unlike bulky devices like chin straps or mouth guards, SnoreStop Throat Spray offers a discreet, hassle-free solution to snoring. Say goodbye to restless nights and the frustration of noisy sleep disturbances—just spray, relax, and wake up refreshed.

Join the millions who have already discovered better sleep with SnoreStop Throat Spray. Try it today and experience the difference!

 FAQs  

Directions for Use:

• Shake Well: Always shake the bottle before each use.
• Spray: At bedtime, spray once under the tongue and once in the back of the throat.
• No Water: Do not take with water.

Treatment Timeline:

• 3-5 Day Course: While some experience results immediately, most users notice improvements within 3-5 nights of consistent use.

Pro Tips for Best Results:

• Use 30 minutes apart from food, water, or other medications.
• Avoid consuming sedatives, alcoholic beverages, or drowsy medicines at bedtime, as these may reduce the effectiveness of SnoreStop.

Start your journey to quieter, more restful nights today with SnoreStop!

* Individual results may vary. SnoreStop does not treat sleep apnea. Results can depend on a variety of factors including overall health, diet, and other lifestyle factors. 

Warnings: Use only as directed. Keep out of reach of children. Do not use it on children under 12 years of age. If pregnant or breastfeeding, ask a doctor before using it. Stop using it and ask a doctor if symptoms do not improve in 7 days. 

Ingredients & Purpose:

• Nux Vomica 4x: helps open constricted pharynx
• Belladonna 6x: helps decongest enlarged tonsils
• Ephedra vulgaris 6x*: helps relieve congestion  
• 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
  
  

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.

Throat Spray Certificate of Analysis

Inactive ingredients: 75% water, 15% Alcohol (100 micro centiliters per spray) 9.9% Glycerin and 0.1% of Potassium sorbate. The glycerin is from vegetable source. 99.7% pure UPS Pharma grade, Natural, and GMO Free.

SnoreStop Extinguisher 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 measurable amount of alkaloids, ephedrine or pseudo - ephedrine. 

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.