FDA.reportPublic FDA data

SnoreStop NasoSpray 60

Manufacturer
Green Pharmaceuticals Inc. | Homeocare Laboratories | HomeoCare Laboratories, Inc. | Coastal Contract Packaging
Effective date
2022-06-16
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 21:51:09

Label at a glance#

ProductSnoreStop NasoSpray 60
Active ingredientSTRYCHNOS NUX-VOMICA SEED, ATROPA BELLADONNA, EPHEDRA DISTACHYA FLOWERING TWIG, GOLDENSEAL, POTASSIUM DICHROMATE, TEUCRIUM MARUM, N.ALPHA.-METHYLHISTAMINE DIHYDROCHLORIDE
Label structure9 sections

Indications and uses

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

Dosage and administration

Adults and children over 5 years old. Shake before each use. At bedtime, spray once into each nostril. Store below 30 degrees C.

Label contents#

Full prescribing information#

Ingredients:

OTC - ACTIVE INGREDIENT SECTION

Nux Vomica 4X,6X, Belladonna 6X, Ephedra 6X, Hydrastis canadensis 6X, Kali bich. 6X, Teucrium marum 6X, Histaminium 12X.

Base:

INACTIVE INGREDIENT SECTION

Benzalkonium chloride, Glycerin, Potassium chloride, Potassium phospate, Purified water, Sodium chloride, Sodium phosphate.

Directions:

INDICATIONS & USAGE SECTION

Adults and children over 5 years old. Shake before each use. At bedtime, spray once into each nostril. Store below 30 degrees C.

Directions: Children over 5 years of age and Adults.

DOSAGE & ADMINISTRATION SECTION

Shake before use. 1. Remove cap and safety clip. 2. Prime by placing nozzle between first and second finger with thumb on the bottom of the bottle. Pump sprayer firmly and quickly until a fine spray appears. 3. Insert spray tip into one nostril, pointing the tip toward the back of the nose. Spray quickly while breathing in through your nose. Clean tip of nozzle after each use and replace cap. Store at room temperatur. May be used up to 4 times per day. Please discard 6 months after first use.

For Maximum Results, use in conjunction with SnoreStop FastTabs or SnoreStop Extinguisher.

Warnings:

WARNINGS SECTION

Use only as directed. Keep this out of reach of children. Do not use on children under 5 years of age. If pregnant or breastfeeding, ask a physician before use. This product does not treat sleep apnea. For sleep apnea, consult with a specialist. If symptoms worsen after 14 days, discontinue use and ask a physician for help.

Comments or Questions?

OTC - QUESTIONS SECTION

Toll free 1-877-SNOREST

email: mal@snorestop.com

Visit: www.snorestop.com

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Uses:

OTC - PURPOSE SECTION

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

NasoSpray 60

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NasoSpray60NasoSpray60

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
61152-199SNORESTOP NASOSPRAY 60 (STRYCHNOS NUX-VOMICA SEED,ATROPA BELLADONNA,EPHEDRA DISTACHYA FLOWERING TWIG,GOLDENSEAL,POTASSIUM DICHROMATE,TEUCRIUM MARUM,HISTAMINE DIHYDROCHLORIDE LIQUID) LIQUID [GREEN PHARMACEUTICALS INC.]4Legacy NDC20221022_f4d26053-32aa-4cc9-8460-556acc38fe33.zip

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
61152-19961152-199-99

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM7N6JUD5X6YIACT
GLYCERINPDC6A3C0OXIACT
POTASSIUM CHLORIDE660YQ98I10IACT
POTASSIUM PHOSPHATE, UNSPECIFIED FORMB7862WZ632IACT
WATER059QF0KO0RIACT
SODIUM CHLORIDE451W47IQ8XIACT
SODIUM PHOSPHATESE337SVY37IACT
STRYCHNOS NUX-VOMICA SEED269XH13919ACTIB
ATROPA BELLADONNAWQZ3G9PF0HACTIB
EPHEDRA DISTACHYA FLOWERING TWIGR55VQ87DP3ACTIB
GOLDENSEALZW3Z11D0JVACTIB
POTASSIUM DICHROMATET4423S18FMACTIB
TEUCRIUM MARUM10464S0TAAACTIB
N.ALPHA.-METHYLHISTAMINE DIHYDROCHLORIDES6S98U0517ACTIB

Source Document#

Source XML · Source PDF

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
462d797b-d5de-e145-e063-6394a90a74d0f4d26053-32aa-4cc9-8460-556acc38fe332025-12-17WarningsExact identifier
spl set id: f4d26053-32aa-4cc9-8460-556acc38fe33

Reported adverse events (FAERS/openFDA)#

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