NerveFix

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: NerveFix
Generic name: ACONITUM NAPELLUS, BELLADONNA, CANTHARIS, FERRUM PHOSPHORICUM, KALI PHOSPHORICUM, MAGNESIA PHOSPHORICA, HYPERICUM PERFORATUM, SPIGELIA ANTHELMIA
Manufacturer: NaturalCare
Product type: HUMAN OTC DRUG
SPL set ID: 92326b54-cac9-4fb2-ae48-120a0dcbbe56
SPL ID: 82b50d4d-b8fa-4977-b91c-9e36dd46f90b
Version: 1
Effective date: 2026-02-03
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 19:59:28

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 · 16 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		NerveFix	openfda.brand_name
generic name		ACONITUM NAPELLUS, BELLADONNA, CANTHARIS, FERRUM PHOSPHORICUM, KALI PHOSPHORICUM, MAGNESIA PHOSPHORICA, HYPERICUM PERFORATUM, SPIGELIA ANTHELMIA	openfda.generic_name
manufacturer name		NaturalCare	openfda.manufacturer_name
ndc	package	70163-0004-1	openfda.package_ndc
ndc	product	70163-0004	openfda.product_ndc
ndc11	package	70163000401	derived:openfda.package_ndc
spl id		82b50d4d-b8fa-4977-b91c-9e36dd46f90b	id
spl set id		92326b54-cac9-4fb2-ae48-120a0dcbbe56	set_id
unii		CI71S98N1Z	openfda.unii
unii		XK4IUX8MNB	openfda.unii
unii		HF539G9L3Q	openfda.unii
unii		3Q034RO3BT	openfda.unii
unii		91GQH8I5F7	openfda.unii
unii		WYT05213GE	openfda.unii
unii		WQZ3G9PF0H	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 worsen or persist for more than 5 days ■ new symptoms appear ■ redness or swelling are present 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 printed foil blister is broken or missing. ■ Store at room temperature (65-80ºF)

Reported adverse events (FAERS/openFDA)#

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