Snore Stop OralSpray
Snore Stop OralSpray is an FDA drug label for the active ingredient ATROPA BELLADONNA, EPHEDRA DISTACHYA FLOWERING TWIG, HISTAMINE, GOLDENSEAL, POTASSIUM DICHROMATE, STRYCHNOS NUX VOMICA SEED, TEUCRIUM MARUM manufactured by Green Pharmaceuticals administered by ORAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20260430.
- Generic name
- ATROPA BELLADONNA, EPHEDRA DISTACHYA FLOWERING TWIG, HISTAMINE, GOLDENSEAL, POTASSIUM DICHROMATE, STRYCHNOS NUX VOMICA SEED, TEUCRIUM MARUM
- Manufacturer
- Green Pharmaceuticals
- Product type
- HUMAN OTC DRUG
- Route
- ORAL
- Dosage form
- N/A
- NDC
- 61152-601
- Application
- N/A
- Label effective
- 20260430
About this product
Snore Stop OralSpray is an FDA-registered drug product whose active ingredient is ATROPA BELLADONNA, EPHEDRA DISTACHYA FLOWERING TWIG, HISTAMINE, GOLDENSEAL, POTASSIUM DICHROMATE, STRYCHNOS NUX VOMICA SEED, TEUCRIUM MARUM. It is labelled by Green Pharmaceuticals taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 61152-601, label effective 20260430. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.
What it is used for
Across FDA labelling, products containing ATROPA BELLADONNA, EPHEDRA DISTACHYA FLOWERING TWIG, HISTAMINE, GOLDENSEAL, POTASSIUM DICHROMATE, STRYCHNOS NUX VOMICA SEED, TEUCRIUM MARUM are most often described in connection with: temporarily relieves, symptoms non-apneic, snoring individual. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Uses Temporarily relieves symptoms of non-apneic snoring. Individual results may vary.
Dosage & Administration
Directions 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.
Warnings
Warnings 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
Recall and safety notices
1 FDA recall record(s) match this product name or manufacturer. A match means the firm or product name appears in the enforcement report; confirm lot numbers and dates against the official FDA notice before acting.
| Recall | Product | Firm | Class | Status | Reported |
|---|---|---|---|---|---|
| D-1165-2022 | SnoreStop NasoSpray, 0.3 FL OZ (9 mL), Green Pharmaceuticals Inc. Camarillo, CA 93012, NDC 61152-199-99, UPC 7 69682 29101 3 | Green Pharmaceuticals, Inc. | Class I | Terminated | 20220706 |
Frequently asked questions
What is Snore Stop OralSpray used for?
Uses Temporarily relieves symptoms of non-apneic snoring. Individual results may vary.
Who makes Snore Stop OralSpray?
Green Pharmaceuticals is the labeler of record for Snore Stop OralSpray.
What form does Snore Stop OralSpray come in?
administered by oral. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.
Is Snore Stop OralSpray prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.
Has Snore Stop OralSpray been recalled?
1 FDA recall record(s) match this product name or manufacturer. Review the recall and safety notices section on this page and confirm lot numbers against the official FDA enforcement report.
Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.
This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.