FDA Label for Snorestop Extinguisher 120

View Indications, Usage & Precautions

Snorestop Extinguisher 120 Product Label

The following document was submitted to the FDA by the labeler of this product Green Pharmaceuticals Inc. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.

Ingredients (Hpus):



Belladonna 6x, Ephedra vulg. 6x, Histaminium hydrochloricum 12x, Hydrastis 6x, Kali bic 6x, Nux vom. 4x, 6x, Teucrium mar. 6x.


Inactive Ingredients:



Alcohol (100 micro centiliters per spray), Glycerin, Potassium sorbate, Purified water (75%).


Uses:



Temporarily relieves symptoms of non-apneic snoring. Individual results may vary.


Warnings:



Warnings: Use only as directed. Keep this out of reach of children. If pregnant or breastfeeding, ask a doctor before use. Stop use and ask a doctor if symptoms do not improve in 7 days.

Use only if tamper resistant seal around the bottle is unbroken.

Store below 77°F (25°C)


Keep Out Of Reach Of Children.



Keep this out of reach of children


Directions:



Adults: Shake bottle before each use. Lift yellow arm up to a right angle.
On first use, prime pump by depressing several times. Spray once under the tongue and once in the back of the throat at bedtime. Do not take with water. Use 30 mins apart from any food, water, or medicine. Please allow3-5 days for initial treatment.

For Maximum Results, use in conjunction with SnoreStop Nasal Spray. May be used up to 4 times a day.

DOES NOT TREAT SLEEP APNEA


Purpose:



Temporarily helps stop or reduce symptoms of non-apneic snoring. Individual results may vary.


* Please review the disclaimer below.