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Cysndra Neuropathy Sprays ARNICA MONTANA 1 [hp_X]/30mL Spray — NDC 87681-0015-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Cysndra Neuropathy Sprays ARNICA MONTANA 1 [hp_X]/30mL Spray — NDC 87681-015-01 (Billing 87681-0015-01)

by Guangzhou Xinhongda Trading Service Co., Ltd. · 1 BOTTLE in 1 BOX / 30 mL in 1 BOTTLE

This is a package of Cysndra Neuropathy Sprays ARNICA MONTANA 1 [hp_X]/30mL Spray from Guangzhou Xinhongda Trading Service Co., Ltd., marketed since Jul 2026 and currently FDA-listed. It is the main listing for this product, which comes in 6 package sizes.

NDC 87681-0015-01
🏷️ FDA NDC (as labeled) 87681-015-01 billing pads the product segment with a zero
This package
Contains30 mL in 1 bottle Pack sizes6 compare ↓
Main listing for product 87681-015 · Also comes in: 30 mL 87681-015-02 30 mL 87681-015-03 30 mL 87681-015-04 30 mL 87681-015-05 30 mL 87681-015-06
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

NDC database record

One package, one record: these facts belong to NDC 87681-015-01 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
87681 labeler · 015 product · 01 package
Package marketed since
Jul 6, 2026
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC-A, from the NDC)
3 8768101501 2
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 87681-015-01
Product NDC 87681-015
11-digit billing NDC 87681001501
UNII O80TY208ZW
SPL Set ID 55ef3a36-cb57-6238-e063-6394a90a7404
DEA schedule Non-controlled
Marketing category UNAPPROVED HOMEOPATHIC
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-07-06
Route TOPICAL
Dosage form SPRAY
Substance ARNICA MONTANA
Why two NDCs? The FDA registers this code as 87681-015-01 — a 5-3-2 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the product segment → 87681-0015-01. Same drug, same package — only the format differs.
Where does this data come from?
Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.

Clinical

🧪 What is this product?

Cysndra Neuropathy Sprays is a homeopathic topical spray containing arnica montana. In homeopathic practice, arnica is traditionally used for minor aches and bruises, though homeopathic products are not evaluated by the FDA for effectiveness and are marketed based on homeopathic tradition rather than established clinical evidence. This product is applied directly to the skin as a spray.

Supplement & herbal interactions

🌿 Drug–supplement interaction checker →
Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.

Pricing

A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.

Price systemPer mLPer package
Retail pharmacies payNADAC · weekly Not in the retail survey — common for institutional, discontinued, or low-volume packs.
Medicaid paysCMS SDUD · 12 mo No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data.
Medicare drug plans payPart D · quarterly No Part D plan price is available for this NDC in our data.
ℹ️
No price is published for this exact package yet. CMS surveys NADAC per package size, so a different pack of the same drug often has one.
Try another pack size: 30 mL 30 mL 30 mL 30 mL 30 mL
Where does this data come from?
NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
87681-0015-01 You're viewing this Main listing 1 BOTTLE in 1 BOX / 30 mL in 1 BOTTLE 2026-07-06 — Active
87681-0015-02 87681-015-02 1 BOTTLE in 1 BOX / 30 mL in 1 BOTTLE 2026-07-06 — Active
87681-0015-03 87681-015-03 1 BOTTLE in 1 BOX / 30 mL in 1 BOTTLE 2026-07-06 — Active
87681-0015-04 87681-015-04 1 BOTTLE in 1 BOX / 30 mL in 1 BOTTLE 2026-07-06 — Active
87681-0015-05 87681-015-05 1 BOTTLE in 1 BOX / 30 mL in 1 BOTTLE 2026-07-06 — Active
87681-0015-06 87681-015-06 1 BOTTLE in 1 BOX / 30 mL in 1 BOTTLE 2026-07-06 — Active

Pack size FAQ

What quantity is in this package?
This package is listed by the FDA — 1 bottle in 1 box / 30 ml in 1 bottle.
What NDC number is used to bill for this package of Cysndra Neuropathy Sprays ARNICA MONTANA 1 [hp_X]/30mL Spray?
Use the 11-digit billing form listed in the identifiers section of this page. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Cysndra Neuropathy Sprays 1 [hp_X]/30mLthis 87681-0015-01 Guangzhou 1 bottle — — FDA listed —
About this product: other versions of the same ingredient, strength and form are listed above, least expensive first, with FDA equivalence ratings where available.
Where does this data come from?
Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.

Availability & generic status

🏛️
2026
On the market since
Jul 2026
📍
2026
Currently FDA-listed
listed with the FDA
🔒
·
No generic listed yet
brand only
ℹ️No FDA-approved generic found

We did not find an FDA-approved generic match for this exact strength, form and route.

Where does this data come from?
Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.

Inactive Ingredients / Excipients

Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • UNII ZY81Z83H0X
    Aloe vera leaf is a plant extract derived from the aloe plant. It is used in medicines as a natural moisturizer and skin-soothing agent in topical formulations.
  • UNII 3XUS85K0RA
    Butylene glycol is a clear liquid derived from petroleum or plants that acts as a humectant, solvent, and preservative booster in medicines. It helps keep formulations stable, dissolve active ingredients, and maintain moisture in topical products.
  • UNII UPY805K99W
    A synthetic compound derived from caprylic acid that works as a preservative and antimicrobial agent to help prevent bacterial and fungal growth in the medicine.
  • UNII 4YS74Q4G4J
    A plant extract from Centella asiatica containing natural compounds called triterpenoids. It's used as an active ingredient in some formulations for its purported skin-supporting properties, though it functions as a botanical additive rather than a structural component of the medicine.
  • UNII PDC6A3C0OX
    Glycerin is a clear, thick liquid derived from plant oils or fats. It acts as a humectant to retain moisture, a sweetener, and a solvent in medications.
  • UNII TM2TZD4G4A
    A plant-derived oily substance used as an emulsifier and solubilizer in medicines. It helps blend water and oil-based ingredients together and improves how the body absorbs certain active drugs.
  • UNII G1L3HT4CMH
    A synthetic compound used in medicines as a preservative and antimicrobial agent. It helps prevent bacterial and fungal growth, extending the product's shelf life.
  • UNII 3K209OP33H
    A beneficial bacterium added to support gut health and digestion. It acts as a probiotic, helping maintain healthy intestinal bacteria balance in the product formulation.
  • UNII N8F53B3R4R
    A synthetic humectant and solvent derived from propane. It draws and holds moisture in the formulation, helping keep the medicine stable and improving texture or flow in liquid and semi-solid products.
  • UNII Z6J799EAJK
    Oat is a cereal grain used in medicines as a filler and binder. It helps give the medication its shape and structure while adding bulk to the formulation.
  • UNII WV9CM0O67Z
    Panthenol is a humectant and skin-conditioning agent derived from pantothenic acid. It's added to medicines to help retain moisture and soothe skin irritation.
  • UNII 7YC686GQ8F
    A synthetic oily substance made from castor oil. It works as a solubilizer and emulsifier to help mix oily and water-based ingredients together in the medicine.
  • UNII 7T1F30V5YH
    A synthetic emulsifier derived from sorbitol and oleic acid. It helps mix oil and water-based ingredients together and keeps them from separating in liquid formulations.
  • UNII KV2JZ1BI6Z
    Pyridoxine is a form of vitamin B6, a water-soluble vitamin. It's added to medicines as a nutritional supplement to help maintain adequate B6 levels in the body.
  • UNII 969IQC5YJU
    A natural plant extract from the rugosa rose flower. It's used in formulations as a fragrance, flavor, or natural colorant to improve the taste, smell, or appearance of the medicine.
  • UNII S2ULN37C9R
    A synthetic chemical compound derived from vanillin that acts as a flavoring agent and fragrance enhancer in medicines. It provides vanilla-like taste and aroma to improve the palatability of oral medications.
  • UNII 059QF0KO0R
    Water is a liquid solvent that dissolves and mixes ingredients together in liquid medicines, syrups, and injections. It helps distribute the active drug evenly throughout the product.

17 inactive ingredients listed in the exact product block matched to this NDC.

The official label also statesWATER 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

Label-section wording can be broader than the structured product block and may mention additional formulation ingredients.

Where does this data come from?
Data sourced from official FDA Structured Product Labeling (SPL) via DailyMed — ingredient classCode="IACT" elements from the exact product block matched by this NDC. Label-section narrative from DailyMed / the openFDA label index is shown separately when available.

Inactive ingredient FAQ

Are inactive ingredients the same for every manufacturer?
No. Inactive ingredients can differ by manufacturer, dosage form, strength, and package / product version.
Why might an inactive ingredient be missing?
Some SPLs do not provide a complete structured inactive-ingredient list, and older or unusual labels may only include the information in narrative text.
Can inactive ingredients matter?
Yes. They can matter for allergies, intolerances, dyes, gluten / lactose concerns, preservatives, and formulation differences — but confirm with a pharmacist or the manufacturer when it’s clinically important.

Manufacturer & labeler

LabelerGuangzhou Xinhongda Trading Service Co., Ltd.
Labeler code87681
First marketedJul 2026
Product typeHuman Otc Drug
Portfolio16 products on file

More NDCs from Guangzhou Xinhongda Trading Service Co., Ltd. labeler code 87681

The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).
Where does this data come from?
Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.

FDA label — Drug Facts FDA SPL

The complete FDA label for this product — the official Drug Facts labeling, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
🎯 Indications and Usage ⏱️ Dosage and Administration ⚠️ Warnings 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Do Not Use 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 9 words ▾

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

⏱️ Dosage and Administration 19 words ▾

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

⚠️ Warnings 47 words ▾

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.

🧪 Active Ingredient 4 words ▾

Arnica Montana 1X HPUS7%

🧪 Inactive Ingredients 42 words ▾

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

🎯 Purpose 6 words ▾

Reduce swelling Pain relief Alleviate inflammatory

📄 Do Not Use 19 words ▾

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

📄 When Using This Product 8 words ▾

When Using this product: Avoid contact with eyes.

📄 Stop Use and Ask a Doctor If 10 words ▾

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

📄 Keep Out of Reach of Children 15 words ▾

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

📄 Package Label / Principal Display Panel 1 words ▾

label1

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

Reported adverse events (FAERS)

Read carefully: FAERS reports are voluntary and unverified. Counts are not incidence, do not establish causation, are subject to reporting bias, and cannot be used to compare one drug to another. Shown for signal context only. Reports for Cysndra Neuropathy Sprays (this brand).

Top reported reactions

Fatigue10
Arthralgia9
Drug Hypersensitivity9
Headache9
Back Pain7
Pruritus7
Cardiac Disorder6

Reporter sex

0 reports
Male · 20%
Female · 78%
Unknown · 1%

Serious outcomes

Hospitalization24
Death4
Disabling2
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 13 0
Most recent year is provisional (FAERS lags ~3 months).
Where does this data come from?
Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.

About this NDC listing & data coverage

Over-the-counter (OTC) product Homeopathic listing

About homeopathic listings

Cysndra Neuropathy Sprays ARNICA MONTANA 1 [hp_X]/30mL SPRAY is listed under the homeopathic marketing category. An NDC listing in this category does not by itself establish FDA approval, and FDA does not evaluate homeopathic products for effectiveness. This page reports the listing data as published.

What data is (and isn’t) available for this NDC — tap to expand
NDC identity (package / product / labeler codes) ✓ Available
Labeler ✓ Available
Product & package description ✓ Available
Marketing category & status ✓ Available
Active ingredient / dosage form / route ✓ Available
FDA label (SPL via DailyMed) ✓ Available
Package photos ✓ Available
Inactive ingredients (structured) ✓ Available
NADAC pharmacy acquisition price (CMS) — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey.
Orange Book / therapeutic-equivalence data — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope.
HCPCS J-code billing crosswalk — Not published for this NDC Most self-administered / retail products have no J-code — that is normal.
Medicaid utilization (CMS SDUD) — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold.
“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.

Questions about this listing

Is this NDC FDA-approved?
An NDC listing does not by itself establish FDA approval — the NDC Directory records that a product is listed with FDA, not that it was reviewed and approved. This listing's marketing category is "Unapproved Homeopathic". Products approved under an application carry an NDA, ANDA, or BLA number.
Why is there no price listed?
The pricing shown on our NDC pages comes from CMS NADAC, a voluntary survey of retail community pharmacy invoices. CMS does not publish a NADAC for every NDC — packages outside the retail survey (institutional and hospital products, bulk packages, discontinued items, and many OTC items) may never receive one. A missing price reflects the survey's scope, not this product's actual cost, and does not mean the product is free or unavailable.
Is the NDC printed on the package the same as the 11-digit billing NDC?
Yes, they identify this exact package in different formats. The form printed on the packaging and shown on DailyMed is the one the FDA registered. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero and the dashes are dropped. The Identity section at the top of this page lists each form of this code.
Is this package still being marketed?
Yes, per the latest FDA NDC Directory data on this page: this package is listed as actively marketed, with no marketing end date reported by Guangzhou Xinhongda Trading Service Co., Ltd.. Listing status can change — the directory data on this page refreshes weekly.
Does this product come in other package sizes?
Yes — the FDA directory lists 5 other package presentations of this same product, including 1 bottle (87681-0015-02), 1 bottle (87681-0015-03), 1 bottle (87681-0015-04). Each has its own NDC and its own page — see the package list near the top of this page.
Who lists this product with the FDA?
Guangzhou Xinhongda Trading Service Co., Ltd. is the labeler of record for this NDC — the company under whose FDA-assigned code the package is listed. The labeler may be the manufacturer itself or a distributor marketing the product under its own code.
Do I need a prescription for this product?
This NDC is listed with FDA as an over-the-counter product, so it does not require a prescription. Follow the package directions, and ask your pharmacist if you are unsure whether it is right for you.
This page identifies an FDA-listed package (the NDC) and reports public regulatory and pricing data about the listing. It is reference information, not a medical recommendation — talk to your pharmacist or prescriber about your own medication.
Where does this data come from?
Listing facts (marketing category, packager status, marketing dates) from the FDA openFDA NDC Directory; label availability from DailyMed; pricing coverage from CMS NADAC; equivalence scope from the FDA Orange Book.
← 87681-0014-01 · Guangzhou 87681-0016-01 · Guangzhou →
For educational and professional reference only — not medical advice. Pricing reflects published NADAC and CMS ASP (free public data) and may differ from your acquisition cost; always verify before billing or dispensing.