SnoreStop® Anti-Snoring Oral Spray

The Natural Way to Quiet Nights

Snoring doesn’t just disrupt your sleep, it disrupts your life. Elbow nudges, tired mornings, and even separate bedrooms can take a toll.

SnoreStop® Oral Spray is the simple, easy to use, natural solution that targets the real cause of snoring: blocked airways in the mouth and in the back of the throat. Just a few quick sprays at bedtime, SnoreStop helps reduce mouth and throat inflammation so air flows freely while drying out built-up mucus so you and your partner can finally enjoy quiet, restful nights.

Why People Choose SnoreStop Oral Spray

• Targets the Root Cause – Reduces swollen tissues in the mouth and in the back of the throat where up to 80% of snoring starts.

• Natural & Non-Habit Forming – Safe to use nightly, with no known side effects or morning grogginess.

• Effortless Routine – Just a few sprays before bed, no uncomfortable mouth guards, strips, or tape.

• Clinically Proven Relief – The only over-the-counter proven snoring solution backed by a peer-reviewed, double blind, placebo controlled published medical study.

• Trusted Quality – FDA-regulated. Made in the USA. Proven Since 1995.

Why It’s Different

Most snoring products are band-aids, strips that tug on your either side of your nose, uncomfortable plastic mouth guards, or tape that forces your mouth shut. SnoreStop works from the inside where the problem really starts.

That means no devices, no discomfort, and no bedtime hassle. Just natural, effective relief you can trust.

Imagine Waking Up To:

✔ Quiet, uninterrupted sleep
✔ No more nudges or midnight frustration
✔ Feeling refreshed and energized in the morning
✔ A happier, better-rested partner

Join the millions who sleep better with SnoreStop Oral Spray.
Effortless. Natural. Proven.

 FAQs  

Directions for Use:

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

Treatment Timeline:

• 5-7 Day Course: While some experience results immediately, most users notice improvements within a minimum of 5 nights of consistent use.

Pro Tips for Best Results:

• Use 30 minutes apart from food, water, or other medications.
  
• Stay hydrated during the day for comfort at night.

• Avoid consuming sedatives, alcoholic beverages, or drowsy medicines at bedtime, as these may reduce the effectiveness of SnoreStop.

Experience better breathing and restful nights within a week of using 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: helps open constricted pharynx
• Belladonna: helps decongest enlarged tonsils
• Ephedra Vulgaris*: helps relieve congestion 
  
• Hydrastis canadensis: helps decongest swollen tongue
• Kali bichromicum: helps relieve stuffy nose
• Teucrium marum: helps open air passages
• Histaminum hydrochloricum: natural antihistamine
  
  

Inactive ingredients: 15% Alcohol (100 micro centiliters per spray) , Glycerin, Potassium sorbate, Purified Water (75%)

Your peace of mind is paramount to us, with a proven safety record since 1995, SnoreStop is your trusted choice. 

SnoreStop Oral Spray is prepared in accordance with the Homeopathic Pharmacopoeia of the United States (HPUS). All ingredients are recognized as GRAS and 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 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.