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Arnica Montana Nartex Arnica montana, Hamamelis Virginiana 1.73 g/29.7g; .0178 g/29.7g Cream, 1 tube — NDC 34666-0001-10 package photo

Arnica Montana Nartex Arnica montana, Hamamelis Virginiana 1.73 g/29.7g; .0178 g/29.7g Cream, 1 tube

by NARTEX LABORATORIOS HOMEOPATICOS SA DE CV · 1 TUBE in 1 CARTON (34666-001-10) / 29.7 g in 1 TUBE
NDC 34666-0001-10
🏷️ FDA NDC (as labeled) 34666-001-10 billing pads the product segment with a zero
This package
Contains1 tube Pack sizes3 compare ↓
Also comes in: 99.79 g 34666-0001-20 74 g 34666-0001-30
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) 34666-001-10
Product NDC 34666-001
11-digit billing NDC 34666000110
UNII O80TY208ZW, T07U1161SV
UPC 0844827000078
SPL Set ID d1407fcf-ae2e-4dac-95bf-6a5f0b21f3a6
DEA schedule Non-controlled
Marketing category UNAPPROVED HOMEOPATHIC
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2007-06-01
Route TOPICAL
Dosage form CREAM
Substance ARNICA MONTANA; HAMAMELIS VIRGINIANA LEAF
Why two NDCs? The FDA registers this code as 34666-001-10 — 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 → 34666-0001-10. 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

LabelerNARTEX LABORATORIOS HOMEOPATICOS SA DE CV
Labeler code34666
First marketedJun 2007
Product typeHuman Otc Drug
Portfolio9 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?

This is an unapproved homeopathic cream applied to the skin containing arnica montana and witch hazel (hamamelis virginiana leaf). In homeopathic practice, these plant extracts are traditionally used for minor skin and bruise concerns, though homeopathic products are not evaluated by the FDA for effectiveness. The claims and uses of homeopathic products are based on homeopathic tradition rather than scientific evidence.

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 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 7EV65EAW6H
    Lanolin is a waxy substance derived from sheep's wool. It's used in medicines as an emollient and skin-conditioning agent to soften formulations and improve spreadability in topical products like creams and ointments.
  • UNII I9O0E3H2ZE
    Paraffin is a waxy, petroleum-derived substance used as a coating, lubricant, and hardening agent in tablets and capsules. It helps protect the medicine from moisture and gives pills a smooth finish.
  • 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 OJ245FE5EU
    Sodium benzoate is a salt derived from benzoic acid, a preservative. It's added to medicines to prevent growth of bacteria, fungi, and other microorganisms that could spoil the product.
  • 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.

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

The official label also statesGlycerin, Lanolin wax, Paraffin wax, Sodium benzoate, Water, White petrolatum

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: 99.79 g 74 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
Arnica Montana Nartex 1.73 g/29.7g; .0178 g/29.7gthis 34666-0001-10 NARTEX 1 tube — — 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

🏛️
2007
On the market since
Jun 2007
📍
2026
Currently FDA-listed
19 years 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
34666-0001-10 You're viewing this 1 TUBE in 1 CARTON (34666-001-10) / 29.7 g in 1 TUBE 2007-06-01 Active
34666-0001-20 1 TUBE in 1 CARTON (34666-001-20) / 99.79 g in 1 TUBE 2021-09-28 Active
34666-0001-30 1 TUBE in 1 CARTON (34666-001-30) / 74 g in 1 TUBE 2022-01-21 Active

Pack size FAQ

What quantity is in NDC 34666-0001-10?
NDC 34666-0001-10 contains 1 tube — 1 tube in 1 carton / 29.7 g in 1 tube.
What is the difference between NDC 34666-0001-10 and NDC 34666-0001-20?
Both are Arnica Montana Nartex Arnica montana, Hamamelis Virginiana 1.73 g/29.7g; .0178 g/29.7g Cream — the drug itself is identical. NDC 34666-0001-10 is the 1 tube package, while NDC 34666-0001-20 is the 1 tube package.
What NDC number is used to bill for this package of Arnica Montana Nartex Arnica montana, Hamamelis Virginiana 1.73 g/29.7g; .0178 g/29.7g Cream?
Bill NDC 34666-0001-10 — the 11-digit billing format is 34666000110. 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 Homeopathic listing

About homeopathic listings

Arnica Montana Nartex Arnica montana, Hamamelis Virginiana 1.73 g/29.7g; .0178 g/29.7g CREAM 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 FDA registers it as 34666-001-10, 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: 34666-0001-10, written without dashes as 34666000110. 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 34666-0001-10, the first segment (34666) is the labeler code FDA assigned to NARTEX LABORATORIOS HOMEOPATICOS SA DE CV; the middle segment (0001) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (10) 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 NARTEX LABORATORIOS HOMEOPATICOS SA DE CV. 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 2 other package presentations of this same product, including 1 tube (34666-0001-20), 1 tube (34666-0001-30). 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?
NARTEX LABORATORIOS HOMEOPATICOS SA DE CV 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 📋 Description
🎯 Indications and Usage 12 words ▾

Uses: Temporary relief for the symptoms of sore muscles, bruises and sprains.

⏱️ Dosage and Administration 25 words ▾

Directions adults and children over 2 years of age: apply generously rubbing into affected area as needed children 2 years of age: consult a physician

⚠️ Warnings 91 words ▾

Warnings For external use only. Do not apply to wounds or damaged skin apply over large areas of the body When using this product avoid contact with eyes or mucous membranes do not bandage tightly Stop use and ask a doctor if symptoms persist for more than 7 days or clear up and occur again within a few days rash develops If pregnant or breast feeding, consult a health professional before use. Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

📦 Storage and Handling 6 words ▾

Other information store at room temperature

🧪 Active Ingredient 37 words ▾

Active Ingredients Each dose contains equal parts of: Arnica montana TINC HPUS Hamamelis virginiana TINC HPUS The letters "HPUS" indicate that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of the Untied States.

🧪 Inactive Ingredients 12 words ▾

Inactive ingredients Glycerin, Lanolin wax, Paraffin wax, Sodium benzoate, Water, White petrolatum

🎯 Purpose 11 words ▾

Purpose Arnica montana TINC HPUS......................Anti-inflammatory/Pain relief Hamamelis virginiana TINC HPUS.............Anti-inflammatory/Pain relief

📋 Description 65 words ▾

Active ingredients are prepared in accordance with the Homeopathic Pharmacopoeia of the United States, and are therefore non-toxic and have no known side effects. Product claims are based on Homeopathic Materia Medica. This product has not been clinically tested by Nartex. Made in Mexico by: NARTEX Laboratorios Homeopaticos, S.A. de C.V. Calz. Lazaro Cardenas 708-770 Ote. Col. Eduardo Guerra Torreon, Coah. Mexico C.P. 27280 www.nartexlabs.com

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 34645-5506-00 · Jianerkang 34666-0007-16 · NARTEX →
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.