SnoreStop Extinguisher 120

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name
SnoreStop Extinguisher 120
Generic name
ATROPA BELLADONNA, EPHEDRA DISTACHYA FLOWERING TWIG, HISTAMINE DIHYDROCHLORIDE, GOLDENSEAL, POTASSIUM DICHROMATE, STRYCHNOS NUX-VOMICA SEED, TEUCRIUM MARUM
Manufacturer
Green Pharmaceuticals Inc
Product type
HUMAN OTC DRUG
SPL set ID
eb534a2f-53ed-3924-e053-2a95a90a0351
SPL ID
2b367965-2a14-dbc4-e063-6294a90a5f74
Version
2
Effective date
2025-01-08
Source export date
2026-09-28
Source partition
11
Source file
https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:18:09
Harmonized routes table
Harmonized routes
ORAL

Warnings cross-check#

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Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings: 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)

Reported adverse events (FAERS/openFDA)#

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