Stage Fright-Fear

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: Stage Fright-Fear
Generic name: ACONITUM NAP., ANACARDIUM, ARG. NIT., ARSENICUM ALB., CYPRIPEDIUM, GELSEMIUM, IGNATIA, KALI CARB., LYCOPODIUM, NAT.MUR., PHOS., SAMBUCUS NIG., SEPIA, STAPHYSAG., STRAMONIUM, TARENTULA HISPANA, THERIDION, PASSIFLORA, VALERIANA
Manufacturer: Newton Laboratories, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 2df84360-dfff-9851-e063-6394a90ad790
SPL ID: 2df84360-e001-9851-e063-6394a90ad790
Version: 1
Effective date: 2025-02-11
Source export date: 2026-10-27
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/a758d73d4d838a965005e6adf01b928e2da86f99be0f8bbaeeb95f3b7acbe418/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 19:58:44

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 · 27 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Stage Fright-Fear	openfda.brand_name
generic name		ACONITUM NAP., ANACARDIUM, ARG. NIT., ARSENICUM ALB., CYPRIPEDIUM, GELSEMIUM, IGNATIA, KALI CARB., LYCOPODIUM, NAT.MUR., PHOS., SAMBUCUS NIG., SEPIA, STAPHYSAG., STRAMONIUM, TARENTULA HISPANA, THERIDION, PASSIFLORA, VALERIANA	openfda.generic_name
manufacturer name		Newton Laboratories, Inc.	openfda.manufacturer_name
ndc	package	55714-2595-1	openfda.package_ndc
ndc	product	55714-2595	openfda.product_ndc
ndc11	package	55714259501	derived:openfda.package_ndc
spl id		2df84360-e001-9851-e063-6394a90ad790	id
spl set id		2df84360-dfff-9851-e063-6394a90ad790	set_id
unii		27YLU75U4W	openfda.unii
unii		00543AP1JV	openfda.unii
unii		QDL83WN8C2	openfda.unii
unii		639KR60Q1Q	openfda.unii
unii		95IT3W8JZE	openfda.unii
unii		451W47IQ8X	openfda.unii
unii		1NM3M2487K	openfda.unii
unii		BQN1B9B9HA	openfda.unii
unii		S7V92P67HO	openfda.unii
unii		86M454L2TT	openfda.unii
unii		JWF5YAW3QW	openfda.unii
unii		U0NQ8555JD	openfda.unii
unii		G6W4F0V8Z3	openfda.unii
unii		CT03BSA18U	openfda.unii
unii		Y0F0BU8RDU	openfda.unii
unii		9Z8D3HEM8L	openfda.unii
unii		CLF5YFS11O	openfda.unii
unii		C88X29Y479	openfda.unii
unii		21Y9GZ1LZA	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.