Home › NDC Lookup › Ingredients › Gemachlich Zuhause Neuropathy Spray. › 76986-0014-03
Gemachlich ZuHause NEUROPATHY Spray. 7 g/100mL Spray, 30 mL — NDC 76986-0014-03 package photo

Gemachlich ZuHause NEUROPATHY Spray. 7 g/100mL Spray, 30 mL

by Guangdong Quadrant Ecological Technology Co., Ltd. · 30 mL in 1 BOTTLE, SPRAY (76986-014-03)
NDC 76986-0014-03
🏷️ FDA NDC (as labeled) 76986-014-03 billing pads the product segment with a zero
This package
Contains30 mL Pack sizes6 compare ↓
Also comes in: 30 ml 76986-0014-01 30 ml 76986-0014-02 30 ml 76986-0014-04 30 ml 76986-0014-05 30 ml 76986-0014-06
OTC On market Non-controlled
🗂️ Data synced 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

🆔 Identity & classification

FDA NDC (as labeled) 76986-014-03
Product NDC 76986-014
11-digit billing NDC 76986001403
UNII O80TY208ZW
UPC 6977863763905
Application # M017
SPL Set ID 425b8259-af38-8d68-e063-6394a90a1120
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2025-10-30
Route TOPICAL
Dosage form SPRAY
Substance ARNICA MONTANA
Why two NDCs? The FDA registers this code as 76986-014-03 — 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 → 76986-0014-03. 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.

🏭 Manufacturer & labeler

LabelerGuangdong Quadrant Ecological Technology Co., Ltd.
FDA applicationM017 (OTC MONOGRAPH DRUG)
Labeler code76986
First marketedOct 2025
Product typeHuman Otc Drug
Portfolio35 products on file
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.

🩺 Clinical

🧪 What is this product?

Gemachlich ZuHause NEUROPATHY Spray is a topical spray product containing arnica montana, an herbal ingredient commonly used in over-the-counter remedies applied directly to the skin. Arnica is traditionally included in topical preparations to address minor muscle soreness, bruising, and discomfort. This product is marketed as an OTC monograph drug, meaning it follows FDA's established rules for its ingredient category rather than undergoing individual product review.

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.

🧪 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 RUE8E6T4NB
    Aloe vera leaf juice is a clear gel extracted from aloe vera plant leaves. It's used in medicines as a lubricant, emollient, and preservative to soothe skin contact and help keep the product stable.
  • UNII 3UVP41R77R
    Avena sativa kernel oil is a natural oil extracted from oat seeds. It's used in medicines as an emollient and skin-conditioning agent to help soften and moisturize the product's texture.
  • 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 7M867G6T1U
    Centella asiatica is a plant extract used in medicines as a skin-conditioning or soothing ingredient. It helps maintain product stability and may support skin comfort in topical formulations.
  • 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 2C1F12C6AP
    A beneficial live bacterium used as a probiotic ingredient. It's included to support the product's probiotic function by promoting beneficial microorganisms in the digestive system.
  • 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 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 239B50Y732
    A synthetic emulsifier derived from sorbitol and lauric acid. It helps blend oil and water-based ingredients together, ensuring even mixing and stable formulation throughout the product's shelf life.
  • 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, Butylene Glycol, Vanillyl Butyl Ether, PEG-40 Hydrogenated Castor Oil, Aloe Barbadensis Leaf Juice Powder, Caprylhydroxamic Acid, Pyridoxine, Glyceryl Caprylate, Avena Sativa (Oat) Kernel Extract, Rosa Rugosa Flower Extract, Centella Asiatica Extract, Hydroxyacetophenone, Lactobacillus Ferment

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.

💲 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.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Gemachlich ZuHause NEUROPATHY Spray. 7 g/100mLthis 76986-0014-03 Guangdong 30 ml — — 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

🏛️
2025
On the market since
Oct 2025
📍
2026
Currently FDA-listed
1 year listed
🔒
·
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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
76986-0014-01 30 mL in 1 BOTTLE, SPRAY (76986-014-01) 2025-10-30 Active
76986-0014-02 30 mL in 1 BOTTLE, SPRAY (76986-014-02) 2025-10-30 Active
76986-0014-03 You're viewing this 30 mL in 1 BOTTLE, SPRAY (76986-014-03) 2025-10-30 Active
76986-0014-04 30 mL in 1 BOTTLE, SPRAY (76986-014-04) 2025-10-30 Active
76986-0014-05 30 mL in 1 BOTTLE, SPRAY (76986-014-05) 2025-10-30 Active
76986-0014-06 30 mL in 1 BOTTLE, SPRAY (76986-014-06) 2025-10-30 Active

Pack size FAQ

What quantity is in NDC 76986-0014-03?
NDC 76986-0014-03 contains 30 mL — 30 ml in 1 bottle, spray.
What is the difference between NDC 76986-0014-03 and NDC 76986-0014-01?
Both are Gemachlich ZuHause NEUROPATHY Spray. 7 g/100mL Spray — the drug itself is identical. NDC 76986-0014-03 is the 30 mL package, while NDC 76986-0014-01 is the 30 ml package.
What NDC number is used to bill for this package of Gemachlich ZuHause NEUROPATHY Spray. 7 g/100mL Spray?
Bill NDC 76986-0014-03 — the 11-digit billing format is 76986001403. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

🧭 About this NDC listing & data coverage

Over-the-counter (OTC) product
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 "Otc Monograph Drug". 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 FDA registers it as 76986-014-03, which is what is printed on the packaging and shown on DailyMed. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero: 76986-0014-03, written without dashes as 76986001403. The Identity section at the top of this page lists every form of this code.
What do the three segments of this NDC mean?
In 76986-0014-03, the first segment (76986) is the labeler code FDA assigned to Guangdong Quadrant Ecological Technology Co., Ltd.; the middle segment (0014) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (03) identifies this exact package size and type. Together they name one specific package of one specific product.
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 Guangdong Quadrant Ecological Technology 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 30 ml (76986-0014-01), 30 ml (76986-0014-02), 30 ml (76986-0014-04). 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?
Guangdong Quadrant Ecological Technology 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.

📄 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 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 9 words ▾

Use Symptomatic treatment of arthritis,neuropathy,tingling, burning and numbness .

⏱️ Dosage and Administration 20 words ▾

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

⚠️ Warnings 53 words ▾

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.

📦 Storage and Handling 26 words ▾

Other information ·If you are using other drugs, please consult your physician or pharmacist before using this product. ·Shielded from light, sealed, stored at room temperature.

🧪 Active Ingredient 5 words ▾

Active Ingredient ARNICA MONTANA 7%

🧪 Inactive Ingredients 42 words ▾

Inactive ingredients Water, Polysorbate 20, Glycerin, Methylpropanediol, Panthenol, Butylene Glycol, Vanillyl Butyl Ether, PEG-40 Hydrogenated Castor Oil, Aloe Barbadensis Leaf Juice Powder, Caprylhydroxamic Acid, Pyridoxine, Glyceryl Caprylate, Avena Sativa (Oat) Kernel Extract, Rosa Rugosa Flower Extract, Centella Asiatica Extract, Hydroxyacetophenone, Lactobacillus Ferment

🎯 Purpose 18 words ▾

Purpose Promotes local blood circulation, adjunctive therapy for Arthritis、Neuropathy,Tingling, Burning and Numbness. Relieves Muscle Pain, Neuralgia, Stiffness,Swelling,Bruising Symptom.

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 76986-0013-01 · Guangdong 76986-0015-01 · Guangdong →
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.