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
2026-10-27
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/2026-10-27/b7a5e61d87a3b8f87f4c3ff7b526bfbf6baf84c840f565574c7d83d4083e2b38/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run
20261027T193451Z
Imported at
2026-10-27 20:50:01
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.