Sick Stopper

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: Sick Stopper
Generic name: ECHINACEA, ACONITUM NAPELLUS, AGARICUS MUSCARIUS, ARALIA QUINQUEFOLIA, BAPTISIA TINCTORIA, BRYONIA, CHELIDONIUM MAJUS, EUPATORIUM PERFOLIATUM, HEPAR SULPHURIS CALCAREUM, LACHESIS MUTUS, LYCOPODIUM CLAVATUM, RHUS TOXICODENDRON, SANGUINARIA CANADENSIS, SULPHUR, THUJA OCCIDENTALIS, BUFO RANA, NUX VOMICA, ANTHRACINUM, INFLUENZINUM, PYROGENIUM
Manufacturer: Newton Laboratories, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 016b7532-8cb6-df55-e063-6394a90abd75
SPL ID: 408063a3-b815-fdee-e063-6294a90af86b
Version: 2
Effective date: 2025-10-06
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 06:18:11

Harmonized routes table
Harmonized routes
ORAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 29 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Sick Stopper	openfda.brand_name
generic name		ECHINACEA, ACONITUM NAPELLUS, AGARICUS MUSCARIUS, ARALIA QUINQUEFOLIA, BAPTISIA TINCTORIA, BRYONIA, CHELIDONIUM MAJUS, EUPATORIUM PERFOLIATUM, HEPAR SULPHURIS CALCAREUM, LACHESIS MUTUS, LYCOPODIUM CLAVATUM, RHUS TOXICODENDRON, SANGUINARIA CANADENSIS, SULPHUR, THUJA OCCIDENTALIS, BUFO RANA, NUX VOMICA, ANTHRACINUM, INFLUENZINUM, PYROGENIUM	openfda.generic_name
manufacturer name		Newton Laboratories, Inc.	openfda.manufacturer_name
ndc	package	55714-2575-1	openfda.package_ndc
ndc	product	55714-2575	openfda.product_ndc
ndc11	package	55714257501	derived:openfda.package_ndc
spl id		408063a3-b815-fdee-e063-6294a90af86b	id
spl set id		016b7532-8cb6-df55-e063-6394a90abd75	set_id
unii		7E889U5RNN	openfda.unii
unii		269XH13919	openfda.unii
unii		8W75VCV53Q	openfda.unii
unii		R9HH0NDE2E	openfda.unii
unii		1314JZ2X6W	openfda.unii
unii		1NT28V9397	openfda.unii
unii		DIF093I037	openfda.unii
unii		29SUH5R3HU	openfda.unii
unii		41LZ22DD4N	openfda.unii
unii		6IO182RP7A	openfda.unii
unii		Q59QU6N72Q	openfda.unii
unii		4N9P6CC1DX	openfda.unii
unii		T7J046YI2B	openfda.unii
unii		70FD1KFU70	openfda.unii
unii		VSW71SS07I	openfda.unii
unii		U0NQ8555JD	openfda.unii
unii		1W0775VX6E	openfda.unii
unii		5EF0HWI5WU	openfda.unii
unii		N9288CD508	openfda.unii
unii		C88X29Y479	openfda.unii
unii		1MBW07J51Q	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

WARNINGS SECTION WARNINGS: Keep out of reach of children. Do not use if tamper-evident seal is broken or missing. If symptoms worsen or persist for more than a few days, consult a doctor. If pregnant or breast-feeding , ask a doctor before use.

Reported adverse events (FAERS/openFDA)#

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