Anxiety HP

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: Anxiety HP
Generic name: ACONITUM NAPELLUS, ARGENTUM NITRICUM, ARSENICUM ALBUM, CALCAREA CARBONICA, IGNATIA AMARA, KALI CARBONICUM, LACHESIS MUTUS, NATRUM MURIATICUM, PHOSPHORUS, PULSATILLA (PRATENSIS), STAPHYSAGRIA, STRAMONIUM
Manufacturer: Energique, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 191393fa-5f36-43c0-a183-09258eef9bda
SPL ID: e471248f-71c3-492f-88ea-072eb4483945
Version: 2
Effective date: 2025-03-20
Source export date: 2026-10-12
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/2026-10-12/a497e765d824a2e2aa9e88d5f0eea2aae9dcba363989e5f163395cda5c3c9dd8/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:45:46

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 · 20 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Anxiety HP	openfda.brand_name
generic name		ACONITUM NAPELLUS, ARGENTUM NITRICUM, ARSENICUM ALBUM, CALCAREA CARBONICA, IGNATIA AMARA, KALI CARBONICUM, LACHESIS MUTUS, NATRUM MURIATICUM, PHOSPHORUS, PULSATILLA (PRATENSIS), STAPHYSAGRIA, STRAMONIUM	openfda.generic_name
manufacturer name		Energique, Inc.	openfda.manufacturer_name
ndc	package	44911-0675-1	openfda.package_ndc
ndc	product	44911-0675	openfda.product_ndc
ndc11	package	44911067501	derived:openfda.package_ndc
spl id		e471248f-71c3-492f-88ea-072eb4483945	id
spl set id		191393fa-5f36-43c0-a183-09258eef9bda	set_id
unii		27YLU75U4W	openfda.unii
unii		00543AP1JV	openfda.unii
unii		95IT3W8JZE	openfda.unii
unii		451W47IQ8X	openfda.unii
unii		1NM3M2487K	openfda.unii
unii		BQN1B9B9HA	openfda.unii
unii		2E32821G6I	openfda.unii
unii		S7V92P67HO	openfda.unii
unii		8E272251DI	openfda.unii
unii		VSW71SS07I	openfda.unii
unii		U0NQ8555JD	openfda.unii
unii		G6W4F0V8Z3	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: Stop use and ask a doctor if symptoms persist for more than 7 days. If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. DO NOT USE IF TAMPER EVIDENT SEAL IS BROKEN OR MISSING Store in a cool, dry place.

Reported adverse events (FAERS/openFDA)#

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