Snorestop Spray
Product Images NDC 61152-600

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Snorestop (NDC 61152-600). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Green Pharmaceuticals Inc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Dosage And Administration (Back Label 03)

This Drug Facts panel for Snorestop oral spray includes warnings such as keeping out of reach of children, age restrictions, and advice on consulting a health professional for sleep apnea or pregnancy. Directions specify spraying twice under the tongue and twice at the back of the throat before bedtime, with usage instructions for children and adults. It also notes tamper-resistant packaging and lists inactive ingredients including citric acid, potassium sorbate, and purified water.*

FDA Label Image

Snorestop Oral Spray (Front Label (003))

Snorestop Oral Spray, a homeopathic natural anti-snoring solution in a 2 fl oz (59 mL) bottle, manufactured by Green Pharmaceuticals Inc. The label highlights quick and easy usage with 400 sprays per container. It features several homeopathic active ingredients such as Belladonna, Cinchona, and Hydrastis canadensis, among others, indicated to temporarily relieve symptoms of non-apneic snoring.*

FDA Label Image

Snorestop (Package)

SnoreStop Oral Spray homeopathic product label indicating it is an anti-snoring solution containing natural ingredients. The label specifies the spray is 2 fluid ounces (59 mL) and contains approximately 400 sprays. The labeler is Green Pharmaceuticals Inc. The design features a green and yellow gradient background with a small illustration of a spray being used orally.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.