FDA.reportPublic FDA data

87681-015 Cysndra Neuropathy Spray

Manufacturer
Guangzhou Xinhongda Trading Service Co., Ltd.
Effective date
2026-07-09
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
daily-update
Hydrated at
2026-07-17 21:45:21

Label at a glance#

ProductCysndra Neuropathy Sprays
Active ingredientARNICA MONTANA
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Arnica Montana 1X HPUS7%

OTC - PURPOSE SECTION

Reduce swelling
Pain relief
Alleviate inflammatory

INDICATIONS & USAGE SECTION

Use: Symptomatic treatmentof arthritis, neuropathy, tingling, burning and numbness.

WARNINGS SECTION


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.

OTC - DO NOT USE SECTION

·by mouth, in nostrils, on wounds or damaged skin.
·if you are under 18 years of age, consult physician.

OTC - WHEN USING SECTION

When Using this product: Avoid contact with eyes.

OTC - STOP USE SECTION

Stop Using and ask a doctor:Discontinue use if irritation occurs.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, get medical help or contact a poison control center immediately.

DOSAGE & ADMINISTRATION SECTION

Apply 1-2 sprays to the affected area, massage it untillabsorbed. Do not use more than 3 times per day.

INACTIVE INGREDIENT SECTION

WATER
POLYSORBATE 20
GLYCERIN
METHYLPROPANEDIOL
PANTHENOL
VANILLYL BUTYL ETHER
CENTELLA ASIATICA EXTRACT
AVENA SATIVA (OAT) KERNEL EXTRACT
ROSA RUGOSA FLOWER EXTRACT
LACTOBACILLUS FERMENT
BUTYLENE GLYCOL
GLYCERYL CAPRYLATE
CAPRYLHYDROXAMIC ACID
HYDROXYACETOPHENONE
BUTYLENE GLYCOL
PEG-40 HYDROGENATED CASTOR OIL
ALOE BARBADENSIS LEAF JUICE POWDER
PYRIDOXINE

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label1label1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87681-01587681-015-01, 87681-015-02, 87681-015-03, 87681-015-04, 87681-015-05, 87681-015-06

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
CAPRYLHYDROXAMIC ACIDUPY805K99WIACT
ARNICA MONTANAO80TY208ZWACTIB
PEG-40 HYDROGENATED CASTOR OIL7YC686GQ8FIACT
CENTELLA ASIATICA TRITERPENOIDS4YS74Q4G4JIACT
METHYLPROPANEDIOLN8F53B3R4RIACT
WATER059QF0KO0RIACT
PANTHENOLWV9CM0O67ZIACT
VANILLYL BUTYL ETHERS2ULN37C9RIACT
OATZ6J799EAJKIACT
ROSA RUGOSA FLOWER969IQC5YJUIACT
PYRIDOXINEKV2JZ1BI6ZIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
ALOE BARBADENSIS LEAF POWDERZY81Z83H0XIACT
LACTOBACILLUS REUTERI F275 STRAIN3K209OP33HIACT
GLYCERYL CAPRYLATETM2TZD4G4AIACT
HYDROXYACETOPHENONEG1L3HT4CMHIACT
POLYSORBATE 207T1F30V5YHIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12026-07-06weekly-update2026-07-17 21:43:12

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
562bc933-2f62-9013-e063-6394a90aac1c55ef3a36-cb57-6238-e063-6394a90a74042026-07-09WarningsExact identifier
spl id: 562bc933-2f62-9013-e063-6394a90aac1c
spl set id: 55ef3a36-cb57-6238-e063-6394a90a7404

Reported adverse events (FAERS/openFDA)#

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