Nervousness - Anxiety

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: Nervousness - Anxiety
Generic name: ACONITUM NAP., AMBRA, ANACARDIUM ORIENTALE, ARG. NIT., ASAFOETIDA, BRYONIA, CHAMOMILLA, CIMICIFUGA, COFFEA CRUDA, CYPRIPEDIUM, GELSEMIUM, HYOSCYAMUS, HYPERICUM, IGNATIA, KALI PHOS., NUX VOM., SAMBUCUS NIG., STRYCHNINUM, THERIDION, VALERIANA, PASSIFLORA
Manufacturer: Newton Laboratories, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 99706ce2-d555-88ca-e053-2a95a90abb4b
SPL ID: b5abb3d5-39f4-3349-e053-2a95a90aada7
Version: 2
Effective date: 2020-12-04
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 20:50:16

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		Nervousness - Anxiety	openfda.brand_name
generic name		ACONITUM NAP., AMBRA, ANACARDIUM ORIENTALE, ARG. NIT., ASAFOETIDA, BRYONIA, CHAMOMILLA, CIMICIFUGA, COFFEA CRUDA, CYPRIPEDIUM, GELSEMIUM, HYOSCYAMUS, HYPERICUM, IGNATIA, KALI PHOS., NUX VOM., SAMBUCUS NIG., STRYCHNINUM, THERIDION, VALERIANA, PASSIFLORA	openfda.generic_name
manufacturer name		Newton Laboratories, Inc.	openfda.manufacturer_name
ndc	package	55714-4783-1	openfda.package_ndc
ndc	product	55714-4783	openfda.product_ndc
ndc11	package	55714478301	derived:openfda.package_ndc
spl id		b5abb3d5-39f4-3349-e053-2a95a90aada7	id
spl set id		99706ce2-d555-88ca-e053-2a95a90abb4b	set_id
unii		CI71S98N1Z	openfda.unii
unii		XK4IUX8MNB	openfda.unii
unii		269XH13919	openfda.unii
unii		3SW678MX72	openfda.unii
unii		H9Y79VD43J	openfda.unii
unii		639KR60Q1Q	openfda.unii
unii		95IT3W8JZE	openfda.unii
unii		W9FZA51AS1	openfda.unii
unii		1NM3M2487K	openfda.unii
unii		4WRK2153H3	openfda.unii
unii		XTC0D02P6C	openfda.unii
unii		T7J046YI2B	openfda.unii
unii		JWF5YAW3QW	openfda.unii
unii		U0NQ8555JD	openfda.unii
unii		CT03BSA18U	openfda.unii
unii		Y0F0BU8RDU	openfda.unii
unii		9Z8D3HEM8L	openfda.unii
unii		CLF5YFS11O	openfda.unii
unii		G0R4UBI2ZZ	openfda.unii
unii		K73E24S6X9	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.