FDA.reportPublic FDA data

Snorestop Oral Spray 59ml

Manufacturer
Green Pharmaceuticals Inc | King Bio Inc
Effective date
2025-08-19
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
full-release
Hydrated at
2026-06-01 02:34:51

Label at a glance#

ProductSnorestop
Active ingredientPRUNUS LAUROCERASUS LEAF, CINCHONA BARK, STRYCHNOS NUX-VOMICA SEED, HYDRASTIS CANADENSIS WHOLE, ATROPA BELLADONNA, HISTAMINE DIHYDROCHLORIDE, TEUCRIUM MARUM, DATURA STRAMONIUM, POTASSIUM DICHROMATE
Label structure11 sections

Indications and uses

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

Dosage and administration

Adults and children 12 years of age and older: Spray twice under the tongue and twice in the back of the throat at bedtime. Use 30 mins apart from any food, water, or medicine. Initially, depress pump until primed. Please allow 3-5 days for initial treatment. Consult a physician for use in children under 12 years of age. Use additionally as needed, up to 4 times per day.

Storage and handling

Tamper resistant for your protection. Use only if safety seal is intact.

Label contents#

Full prescribing information#

Ingredients (HPUS):

OTC - ACTIVE INGREDIENT SECTION

Snorestop Oral SpraySnorestop Oral SprayEqual volumes of each HPUS ingredient in 10X, 30X.

Nux vomica 10X, 20X, & 30X, Belladonna 10X, 20X, & 30X, Hydrastis canadensis 10X, 20X, & 30X, Kali bichromicum 10X, 20X, & 30X, Teucrium marum 10X, 20X, & 30X, Histaminum hydrochloricum 10X, 20X, & 30X, Laurocerasus 10X, 20X, & 30X, Cinchona10X, 20X, & 30X, Stramonium 10X, 20X, & 30X.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Citric Acid
Potassium Sorbate
USP Purified Water

Uses:

INDICATIONS & USAGE SECTION

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

Warnings:

WARNINGS SECTION

Use only as directed. Keep out of reach of children.
Do not use on children under 12 years of age.
This product does not treat sleep apnea. If you have sleep apnea,consult a health professional.
If pregnant or breastfeeding, ask a health professional before use.
Stop use and ask a doctor if symptoms do not improve in 7 days.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Directions:

DOSAGE & ADMINISTRATION SECTION

Dosage and AdministrationDosage and AdministrationAdults and children 12 years of age and older: Spray twice under the tongue and twice in the back of the throat at bedtime.

Use 30 mins apart from any food, water, or medicine.

Initially, depress pump until primed.

Please allow 3-5 days for initial treatment.

Consult a physician for use in children under 12 years of age.

Use additionally as needed, up to 4 times per day.

Purpose:

OTC - PURPOSE SECTION

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

Other information

STORAGE AND HANDLING SECTION

Tamper resistant for your protection. Use only if safety seal is intact.

RECENT MAJOR CHANGES SECTION

Indications and Usage

Warnings and Precautions

Dosage and Administration

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SnoreStopSnoreStopSnorestop Oral Spray

A Natural Anti-Snoring solution

Quick & Easy

Contains 400 Sprays

Homeopathic 2fl oz (59ml)

UPC 7 69682 40015 6

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
e2db08c6-133f-4f4f-afb4-e90a2418d6f6Product name120230320
ce6d5c06-3ae0-18a6-d5b3-8cd3cc0f8906Product name720210625
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
11ed6f83-cdd2-4637-8379-b1a1d3ae3cdeProduct name120181101
86c45a79-b9f0-4476-a27c-6e10db098497Product name120180125
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61152-600-59Snorestop59 mL in 1 BOTTLE, SPRAYSPRAY598

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
61152-60061152-600-59

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
PRUNUS LAUROCERASUS LEAFF26P2D4757ACTIB
CINCHONA BARK292E43P4I9ACTIB
STRYCHNOS NUX-VOMICA SEED269XH13919ACTIB
HYDRASTIS CANADENSIS WHOLER763EBH88TACTIB
POTASSIUM SORBATE1VPU26JZZ4IACT
WATER059QF0KO0RIACT
ATROPA BELLADONNAWQZ3G9PF0HACTIB
HISTAMINE DIHYDROCHLORIDE3POA0Q644UACTIB
TEUCRIUM MARUM10464S0TAAACTIB
DATURA STRAMONIUMG6W4F0V8Z3ACTIB
POTASSIUM DICHROMATET4423S18FMACTIB
ANHYDROUS CITRIC ACIDXF417D3PSLIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
SnorestopNUX VOMICA, BELLADONNA, HYDRASTIS CANADENSIS, KALI BICHROMICUM, TEUCRIUM MARUM, HISTAMINUM HYDROCHLORICUM, LAUROCERASUS, CINCHONA, STRAMONIUMGreen Pharmaceuticals Inc37f4ea81-691f-597b-e063-6294a90a84bd2025-08-19WarningsExact identifier
ndc (package): 61152-600-59
ndc (product): 61152-600
ndc11 (package): 61152060059
spl id: 3cbe7366-0da4-dfc9-e063-6394a90addbd
spl set id: 37f4ea81-691f-597b-e063-6294a90a84bd

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.