FDA.reportPublic FDA data

Snore Stop Oral Spray

Manufacturer
Green Pharmaceuticals
Effective date
2026-04-30
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-07-18 05:11:04

Label at a glance#

ProductSnore Stop OralSpray
Active ingredientSTRYCHNOS NUX-VOMICA SEED, HISTAMINE, POTASSIUM DICHROMATE, GOLDENSEAL, ATROPA BELLADONNA, TEUCRIUM MARUM, EPHEDRA DISTACHYA FLOWERING TWIG
Label structure9 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 at the back of the throat at bedtime. Use 30 minutes 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: Store upright in a cool, dry plac...

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION


Nux vom. 4X, 6X, HPUS....helps open constricted pharynx

Belladonna 6X HPUS....helps decongest enlarged tonsils

Ephedra Vulg. 6X HPUS....helps relieve nasal congestion

Hydrastis 6X HPUS....helps decongest swollen tongue

Kali bic. 6X HPUS....helps relieve stuffy nose

Teucrium mar. 6X HPUS....helps open air passages

Histaminium hydrochlor 12X HPUS....antihistamine

The letters HPUS indicate that this ingredient is officially included in the Homeopathic Pharmacopoeia of the United States.

Dilution scale: 6X is equal to one part million.

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.

Keep out of the reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children

Warnings

WARNINGS SECTION

Warnings

  • 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

Directions

DOSAGE & ADMINISTRATION SECTION

  • Adults and children 12 years of age and older: Spray twice under the tongue and twice at the back of the throat at bedtime.
  • Use 30 minutes 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: Store upright in a cool, dry place and away from direct sunlight.

Other Information

OTC - DO NOT USE SECTION

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

OTC - PURPOSE SECTION

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

SnoreStop Oral Spray

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Snore Stop Throat SpraySnore Stop Throat Spray
SnoreStop_Label_Image.jpg

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130769682400156GTIN-13: 0769682400156
EAN-13: 0769682400156
GTIN-12: 769682400156
UPC-A: 769682400156
GTIN storage (14 digits): 00769682400156		SnoreStop_Label_Image.jpg
QR code linkQR Codesnorestop.com/pages/faqsSnoreStop_Label_Image.jpg

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
61152-60161152-601-59

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
STRYCHNOS NUX-VOMICA SEED269XH13919ACTIB
POTASSIUM SORBATE1VPU26JZZ4IACT
HISTAMINE820484N8I3ACTIB
POTASSIUM DICHROMATET4423S18FMACTIB
GOLDENSEALZW3Z11D0JVACTIB
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT
ATROPA BELLADONNAWQZ3G9PF0HACTIB
TEUCRIUM MARUM10464S0TAAACTIB
EPHEDRA DISTACHYA FLOWERING TWIGR55VQ87DP3ACTIB

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
Snore Stop OralSprayATROPA BELLADONNA, EPHEDRA DISTACHYA FLOWERING TWIG, HISTAMINE, GOLDENSEAL, POTASSIUM DICHROMATE, STRYCHNOS NUX VOMICA SEED, TEUCRIUM MARUMGreen Pharmaceuticals544dda7f-c748-eda7-e063-6394a90ab0912026-04-30WarningsExact identifier
ndc (package): 61152-601-59
ndc (product): 61152-601
ndc11 (package): 61152060159
spl id: 544dda7f-c749-eda7-e063-6394a90ab091
spl set id: 544dda7f-c748-eda7-e063-6394a90ab091

Reported adverse events (FAERS/openFDA)#

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