Cysndra Neuropathy Sprays

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: Cysndra Neuropathy Sprays
Generic name: ARNICA MONTANA
Manufacturer: Guangzhou Xinhongda Trading Service Co., Ltd.
Product type: HUMAN OTC DRUG
SPL set ID: 55ef3a36-cb57-6238-e063-6394a90a7404
SPL ID: 562bc933-2f62-9013-e063-6394a90aac1c
Version: 2
Effective date: 2026-07-09
Source export date: 2026-09-28
Source partition: 2
Source file: https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:15:18

Harmonized routes table
Harmonized routes
TOPICAL

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 · 19 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Cysndra Neuropathy Sprays	openfda.brand_name
generic name		ARNICA MONTANA	openfda.generic_name
manufacturer name		Guangzhou Xinhongda Trading Service Co., Ltd.	openfda.manufacturer_name
ndc	package	87681-015-05	openfda.package_ndc
ndc	package	87681-015-02	openfda.package_ndc
ndc	package	87681-015-06	openfda.package_ndc
ndc	package	87681-015-03	openfda.package_ndc
ndc	package	87681-015-04	openfda.package_ndc
ndc	package	87681-015-01	openfda.package_ndc
ndc	product	87681-015	openfda.product_ndc
ndc11	package	87681001501	derived:openfda.package_ndc
ndc11	package	87681001504	derived:openfda.package_ndc
ndc11	package	87681001506	derived:openfda.package_ndc
ndc11	package	87681001505	derived:openfda.package_ndc
ndc11	package	87681001502	derived:openfda.package_ndc
ndc11	package	87681001503	derived:openfda.package_ndc
spl id		562bc933-2f62-9013-e063-6394a90aac1c	id
spl set id		55ef3a36-cb57-6238-e063-6394a90a7404	set_id
unii		O80TY208ZW	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

For external use only. Keep away from fire and flame. Ask a doctor before use if pregnant or nursing. Prohibited for those who are allergic to this product. Allergic persons should be cautious. Prohibit the use of this product when the properties of the product have changed.

Reported adverse events (FAERS/openFDA)#

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