FDA.reportPublic FDA data

SnoreStop Throat Spray 120

Manufacturer
Green Pharmaceuticals Inc | Homeocare Laboratories
Effective date
2025-01-08
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:30:10

Label at a glance#

ProductSnoreStop Extinguisher 120
Active ingredientATROPA BELLADONNA, EPHEDRA DISTACHYA FLOWERING TWIG, HISTAMINE DIHYDROCHLORIDE, GOLDENSEAL, POTASSIUM DICHROMATE, STRYCHNOS NUX-VOMICA SEED, TEUCRIUM MARUM
Label structure10 sections

Indications and uses

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

Dosage and administration

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 time...

Storage and handling

Use only if tamper resistant seal around the bottle is unbroken. Store below 77°F (25°C) Distributed by Green Pharmaceuticals, Camarillo, CA 93012, USA. Questions? Call 1-877-SNORESTOP or visit www.snorestop.com

Label contents#

Full prescribing information#

Ingredients (HPUS):

OTC - ACTIVE INGREDIENT SECTION

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

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

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

Uses:

INDICATIONS & USAGE SECTION

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

Warnings:

WARNINGS SECTION

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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep this out of reach of children

Directions:

DOSAGE & ADMINISTRATION SECTION

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:

OTC - PURPOSE SECTION

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

Other information

STORAGE AND HANDLING SECTION

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

Store below 77°F (25°C)

Distributed by Green Pharmaceuticals, Camarillo, CA 93012, USA.
Questions? Call 1-877-SNORESTOP or visit www.snorestop.com

Questions?

OTC - QUESTIONS SECTION

Questions? Call 1-877-SNORESTOP or visit www.snorestop.com

SnoreStop Extinguisher 120

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 61152-400-15NDC 61152-400-15

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61152-400-15SnoreStop Extinguisher 12018 mL in 1 BOTTLE, SPRAYSPRAY182

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
61152-400SNORESTOP EXTINGUISHER 120 (ATROPA BELLADONNA, EPHEDRA DISTACHYA FLOWERING TWIG, HISTAMINE DIHYDROCHLORIDE, GOLDENSEAL, POTASSIUM DICHROMATE, STRYCHNOS NUX-VOMICA SEED, TEUCRIUM MARUM) SPRAY [GREEN PHARMACEUTICALS INC]2Current NDC, Legacy NDC, 1 package rows20250110_eb534a2f-53ed-3924-e053-2a95a90a0351.zip

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
61152-40061152-400-15

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MIACT
GLYCERINPDC6A3C0OXIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
WATER059QF0KO0RIACT
ATROPA BELLADONNAWQZ3G9PF0HACTIB
EPHEDRA DISTACHYA FLOWERING TWIGR55VQ87DP3ACTIB
HISTAMINE DIHYDROCHLORIDE3POA0Q644UACTIB
GOLDENSEALZW3Z11D0JVACTIB
POTASSIUM DICHROMATET4423S18FMACTIB
STRYCHNOS NUX-VOMICA SEED269XH13919ACTIB
TEUCRIUM MARUM10464S0TAAACTIB

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
SnoreStop Extinguisher 120ATROPA BELLADONNA, EPHEDRA DISTACHYA FLOWERING TWIG, HISTAMINE DIHYDROCHLORIDE, GOLDENSEAL, POTASSIUM DICHROMATE, STRYCHNOS NUX-VOMICA SEED, TEUCRIUM MARUMGreen Pharmaceuticals Inceb534a2f-53ed-3924-e053-2a95a90a03512025-01-08WarningsExact identifier
ndc (package): 61152-400-15
ndc (product): 61152-400
ndc11 (package): 61152040015
spl id: 2b367965-2a14-dbc4-e063-6294a90a5f74
spl set id: eb534a2f-53ed-3924-e053-2a95a90a0351

Reported adverse events (FAERS/openFDA)#

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