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Gemachlich ZuHause NEUROPATHY SOLID Ointment. 7 g/100g Ointment, 20 g — NDC 76986-0013-01 package photo

Gemachlich ZuHause NEUROPATHY SOLID Ointment. 7 g/100g Ointment, 20 g

by Guangdong Quadrant Ecological Technology Co., Ltd. · 20 g in 1 TUBE (76986-013-01)
NDC 76986-0013-01
🏷️ FDA NDC (as labeled) 76986-013-01 billing pads the product segment with a zero
This package
Contains20 g Pack sizes6 compare ↓
Also comes in: 20 g 76986-0013-02 20 g 76986-0013-03 20 g 76986-0013-04 20 g 76986-0013-05 20 g 76986-0013-06
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) 76986-013-01
Product NDC 76986-013
11-digit billing NDC 76986001301
UNII O80TY208ZW
UPC 6977863763875
Application # M017
SPL Set ID 425b1b9d-c33a-05e9-e063-6394a90a97a6
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 OINTMENT
Substance ARNICA MONTANA
Why two NDCs? The FDA registers this code as 76986-013-01 — 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 → 76986-0013-01. 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.

🏭 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 Solid Ointment is a topical ointment containing arnica montana, an herbal ingredient commonly used in over-the-counter products for minor muscle and joint discomfort. This product is marketed as an OTC monograph drug, meaning it follows established FDA guidelines for its product category rather than undergoing individual product approval. Arnica is typically applied to the skin and is traditionally used to help ease minor aches and soreness.

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 TR046Y3K1G
    A liquid alcohol derived from petroleum or plant sources. It acts as a solvent and humectant in medicines, helping dissolve active ingredients and retain moisture in the formulation.
  • UNII 933ANU3H2S
    12-Hydroxystearic acid is a fatty acid derived from plant or animal oils. It works as a thickener and emulsifier in medicines, helping blend ingredients together and give the product a smooth, stable 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 5TJD82A1ET
    A cooling crystalline substance made synthetically that is added to medicines as a fragrance, flavoring agent, and mild local irritant to produce a cooling or warming sensation on the skin or mucous membranes.
  • UNII BZ2O8A84A4
    Ceralifimod is a synthetic compound used as an active pharmaceutical ingredient in certain immunomodulatory medicines. It functions to help regulate immune system responses rather than serving a traditional excipient role like binding or flavoring.
  • UNII Q1LS2UJO3A
    Ceresin is a purified mineral wax derived from ozocerite. It functions as a binding agent, thickener, and coating material in medicines to help hold ingredients together and provide texture or protective coating.
  • UNII 936JST6JCN
    Cetyl alcohol is a waxy, fatty substance derived from plant or animal sources. It acts as an emulsifier and thickener in medicines, helping blend oil and water components and giving products a smooth, creamy texture.
  • UNII 25P9H3QU5E
    A natural oil extracted from mandarin orange peel. It serves as a flavoring agent and fragrance ingredient to improve the taste and smell of the medicine.
  • UNII 603RP8TB9A
    A wax-like substance made from stearic acid and ethylene. It works as a glidant and lubricant to help the medicine flow smoothly during manufacturing and to prevent sticking in tablets or capsules.
  • UNII WL0328HX19
    A natural plant-based wax derived from candelilla shrub leaves. It acts as a coating agent, hardener, and texture modifier to control how quickly the medicine releases and to improve the tablet or capsule's appearance and stability.
  • UNII 535G2ABX9M
    Fucus vesiculosus is a brown seaweed that serves as a thickener, binder, and emulsifier in medicines. It helps create smooth texture and hold ingredients together in liquid and semi-solid 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 FCZ5MH785I
    A waxy substance made from glycerin and stearic acid. It works as an emulsifier to help mix oil and water ingredients together, and as a thickener to give the medicine its proper texture and consistency.
  • 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 XK4IUX8MNB
    Hypericum perforatum, also known as St. John's Wort, is a plant extract used in some medicines. It may serve as an active botanical ingredient or flavoring agent depending on the formulation.
  • UNII T5L8T28FGP
    Mineral oil is a clear, odorless liquid derived from crude oil. It acts as a lubricant and emollient in medications, helping pills slide smoothly during manufacturing and aiding moisture retention in topical products.
  • UNII 4T6H12BN9U
    Petrolatum is a purified mineral oil-based jelly derived from petroleum. In medicines, it acts as an emollient, lubricant, and moisture barrier to soften skin, reduce friction, and help prevent water loss from formulations.
  • UNII 2KR89I4H1Y
    Stearyl alcohol is a waxy, fatty substance derived from natural oils or made synthetically. It acts as an emulsifier and thickener in medicines, helping mix ingredients together and give the product the right texture.
  • UNII H5KI1C3YTV
    A plant-derived polymer made from sucrose that has been chemically modified. It functions as a film-coating agent and viscosity modifier to control how quickly the medicine dissolves and releases its active ingredients.
  • 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.

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

The official label also statesPetrolatum,Mineral Oil,Ozokerite,Far-Infrared Ceramic Powder,Cera Microcristallina,Stearyl Alcohol,Glyceryl Stearate,Hypericum Perforatum Oil,Camphor,Sucrose Acetate Isobutyrate,Vanillyl Butyl Ether,Cetyl Alcohol,Euphorbia Cerifera (Candelilla) Wax,Hydroxystearic Acid,Water,Butylene Glycol,Citrus Reticulata (Tangerine) Fruit Extract,Glycerin,Fucus Vesiculosus Extract,1,2-Hexanediol,Hydroxyacetophenone

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 gPer 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: 20 g 20 g 20 g 20 g 20 g
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 SOLID Ointment. 7 g/100gthis 76986-0013-01 Guangdong 20 g — — 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
76986-0013-01 You're viewing this 20 g in 1 TUBE (76986-013-01) 2025-10-30 Active
76986-0013-02 20 g in 1 TUBE (76986-013-02) 2025-10-30 Active
76986-0013-03 20 g in 1 TUBE (76986-013-03) 2025-10-30 Active
76986-0013-04 20 g in 1 TUBE (76986-013-04) 2025-10-30 Active
76986-0013-05 20 g in 1 TUBE (76986-013-05) 2025-10-30 Active
76986-0013-06 20 g in 1 TUBE (76986-013-06) 2025-10-30 Active

Pack size FAQ

What quantity is in NDC 76986-0013-01?
NDC 76986-0013-01 contains 20 g — 20 g in 1 tube.
What is the difference between NDC 76986-0013-01 and NDC 76986-0013-02?
Both are Gemachlich ZuHause NEUROPATHY SOLID Ointment. 7 g/100g Ointment — the drug itself is identical. NDC 76986-0013-01 is the 20 g package, while NDC 76986-0013-02 is the 20 g package.
What NDC number is used to bill for this package of Gemachlich ZuHause NEUROPATHY SOLID Ointment. 7 g/100g Ointment?
Bill NDC 76986-0013-01 — the 11-digit billing format is 76986001301. 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 76986-013-01, 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: 76986-0013-01, written without dashes as 76986001301. 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 76986-0013-01, the first segment (76986) is the labeler code FDA assigned to Guangdong Quadrant Ecological Technology Co., Ltd.; the middle segment (0013) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (01) 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 20 g (76986-0013-02), 20 g (76986-0013-03), 20 g (76986-0013-04). 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 8 words ▾

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

⏱️ Dosage and Administration 13 words ▾

Directions Apply to the affected areas 2-3 times daily, massage it till absorbed.

⚠️ 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 27 words ▾

Inactive ingredients Petrolatum,Mineral Oil,Ozokerite,Far-Infrared Ceramic Powder,Cera Microcristallina,Stearyl Alcohol,Glyceryl Stearate,Hypericum Perforatum Oil,Camphor,Sucrose Acetate Isobutyrate,Vanillyl Butyl Ether,Cetyl Alcohol,Euphorbia Cerifera (Candelilla) Wax,Hydroxystearic Acid,Water,Butylene Glycol,Citrus Reticulata (Tangerine) Fruit Extract,Glycerin,Fucus Vesiculosus Extract,1,2-Hexanediol,Hydroxyacetophenone

🎯 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 ↗
← 76986-0012-01 · Guangdong 76986-0014-01 · 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.