Anxiety Relief

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 Relief
Generic name: ACONITUM NAPELLUS, ARGENTUM NITRICUM, ARSENICUM ALBUM, AURUM METALLICUM, GELSEMIUM SEMPERVIRENS, HYOSCYAMUS NIGER, IGNATIA AMARA, KALI CARBONICUM, MOSCHUS, NATRUM MURIATICUM, PIPER METHYSTICUM
Manufacturer: NaturalCare
Product type: HUMAN OTC DRUG
SPL set ID: 9f982e89-655c-49be-85d8-4099a02ed021
SPL ID: ff795cc1-d497-42f0-af22-94790ecc7e5f
Version: 1
Effective date: 2026-04-15
Source export date: 2026-09-28
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:20:03

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 · 21 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Anxiety Relief	openfda.brand_name
generic name		ACONITUM NAPELLUS, ARGENTUM NITRICUM, ARSENICUM ALBUM, AURUM METALLICUM, GELSEMIUM SEMPERVIRENS, HYOSCYAMUS NIGER, IGNATIA AMARA, KALI CARBONICUM, MOSCHUS, NATRUM MURIATICUM, PIPER METHYSTICUM	openfda.generic_name
manufacturer name		NaturalCare	openfda.manufacturer_name
ndc	package	70163-0047-1	openfda.package_ndc
ndc	package	70163-0047-2	openfda.package_ndc
ndc	product	70163-0047	openfda.product_ndc
ndc11	package	70163004701	derived:openfda.package_ndc
ndc11	package	70163004702	derived:openfda.package_ndc
spl id		ff795cc1-d497-42f0-af22-94790ecc7e5f	id
spl set id		9f982e89-655c-49be-85d8-4099a02ed021	set_id
unii		BOW48C81XP	openfda.unii
unii		8KFK4W7KP7	openfda.unii
unii		639KR60Q1Q	openfda.unii
unii		95IT3W8JZE	openfda.unii
unii		451W47IQ8X	openfda.unii
unii		1NM3M2487K	openfda.unii
unii		79Y1949PYO	openfda.unii
unii		BQN1B9B9HA	openfda.unii
unii		4WRK2153H3	openfda.unii
unii		S7V92P67HO	openfda.unii
unii		U0NQ8555JD	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 30 days ■ symptoms become more severe 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 missing or open. ■ Store at room temperature (65-80ºF)

Reported adverse events (FAERS/openFDA)#

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