Sciatica-Nerve Care

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: Sciatica-Nerve Care
Generic name: ACONITUM NAP., AMMONIUM BENZOICUM, ARSENICUM ALB., BENZOICUM ACIDUM, BRYONIA, CAUSTICUM, CINCHONA, COLCHICUM, GNAPHALIUM POLYCEPHALUM, IRIS VERSICOLOR, KALI IOD., LEDUM, LITHIUM CARB., NUX VOM., PHYTOLACCA, RHUS TOXICODERON, RUTA, SAMBUCUS NIG., STRYCHNINUM, HYPERICUM, URTICA UR
Manufacturer: Newton Laboratories, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 9cbda496-ef30-18af-e053-2995a90a2321
SPL ID: 2dcfec4c-76f4-0efd-e063-6394a90acdf6
Version: 2
Effective date: 2025-02-10
Source export date: 2026-09-28
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/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:26:33

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		Sciatica-Nerve Care	openfda.brand_name
generic name		ACONITUM NAP., AMMONIUM BENZOICUM, ARSENICUM ALB., BENZOICUM ACIDUM, BRYONIA, CAUSTICUM, CINCHONA, COLCHICUM, GNAPHALIUM POLYCEPHALUM, IRIS VERSICOLOR, KALI IOD., LEDUM, LITHIUM CARB., NUX VOM., PHYTOLACCA, RHUS TOXICODERON, RUTA, SAMBUCUS NIG., STRYCHNINUM, HYPERICUM, URTICA UR	openfda.generic_name
manufacturer name		Newton Laboratories, Inc.	openfda.manufacturer_name
ndc	package	55714-2513-1	openfda.package_ndc
ndc	product	55714-2513	openfda.product_ndc
ndc11	package	55714251301	derived:openfda.package_ndc
spl id		2dcfec4c-76f4-0efd-e063-6394a90acdf6	id
spl set id		9cbda496-ef30-18af-e053-2995a90a2321	set_id
unii		877L01IZ0P	openfda.unii
unii		11E6VI8VEG	openfda.unii
unii		XK4IUX8MNB	openfda.unii
unii		269XH13919	openfda.unii
unii		DD5FO1WKFU	openfda.unii
unii		H9Y79VD43J	openfda.unii
unii		993QHL78E6	openfda.unii
unii		8SKN0B0MIM	openfda.unii
unii		N94C2U587S	openfda.unii
unii		IHN2NQ5OF9	openfda.unii
unii		6IO182RP7A	openfda.unii
unii		S7V92P67HO	openfda.unii
unii		S003A158SB	openfda.unii
unii		T7J046YI2B	openfda.unii
unii		36XQ854NWW	openfda.unii
unii		U0NQ8555JD	openfda.unii
unii		1C4QK22F9J	openfda.unii
unii		CT03BSA18U	openfda.unii
unii		X43D4L3DQC	openfda.unii
unii		2BMD2GNA4V	openfda.unii
unii		AC80WD7GPF	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.