SnoreStop® for Pets Tablets
It's cute - until it's 2am and you just want to SLEEP!
Who would have ever thought that you would be here looking for help to muzzle your pet's snoring?!
But here you are - and we are glad you're here. You get to join our other pet owners/customers so you can get some sleep too.
Directions: Place one tablet in a treat or crush it in the water bowl before your nightly walk around the neighborhood. You can double the dosage at your discretion.
3-5 DAY TREATMENT COURSE: Most experience a result right away while others get results within 3-5 nights. Use SnoreStop for Pets at bedtime 30 mins apart from any other medicine.
Warnings: Use only as directed. Keep out of reach of children. If after 7 days symptoms worsen, discontinue use and consult with a veterinarian.
* Individual results may vary. Results can depend on a variety of factors including overall health, diet, and other lifestyle factors.
Give Us Your Opinion, and Share a Selfie of Your Four-Legged Family Member, Too!
We want to hear your opinion of our products, so please tell us your story.
We love pictures of happy, well-rested pets and their owners!
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- Teucrium marum 6X: helps open air passages
- Histaminum 12X: natural antihistamine
Inactive ingredients: Lactose, Cellulose, Dextrose, Croscamellose sodium, Magnesium stearate (in each 300 mg tablet).
SnoreStop for Pets tablets 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 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. 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 Administration.