NDC 54532-0024-06 — Hevert Trauma Roll-On Arnica Montana Root

🆔 Identity & classification

FDA NDC (as labeled) 54532-0024-6

Product NDC 54532-0024

11-digit billing NDC 54532002406

UNII MUE8Y11327, 2HU33I03UY, 18E7415PXQ, T7S323PKJS, XK4IUX8MNB, 55862Q3XEU +2 more

SPL Set ID dce69e3b-e080-459c-a444-4f84322a7f89

DEA schedule Non-controlled

Marketing category UNAPPROVED HOMEOPATHIC

Marketing status On market

FDA listing status Listed (active directory)

Marketing start 2016-04-01

Route TOPICAL

Dosage form GEL

Substance ARNICA MONTANA ROOT; BELLIS PERENNIS WHOLE; CALENDULA OFFICINALIS FLOWERING TOP; HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; HYPERICUM PERFORATUM WHOLE; ACHILLEA MILLEFOLIUM FLOWERING TOP; RUTA GRAVEOLENS FLOWERING TOP; COMFREY ROOT

Why two NDCs? The FDA registers this code as 54532-0024-6 — a 5-4-1 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 package segment → 54532-0024-06. 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

LabelerHevert Arzneimittel GmbH & Co KG

Labeler code54532

First marketedApr 2016

Product typeHuman Otc Drug

Portfolio6 products on file

🔎 All NDCs from Hevert Arzneimittel GmbH & Co KG

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 a topical gel marketed as a homeopathic product containing eight plant-derived ingredients including arnica, calendula, comfrey, and hypericum. In homeopathic practice, these substances are traditionally used for topical application to minor skin concerns and bruising, though homeopathic products are not evaluated by the FDA for effectiveness and are marketed based on homeopathic tradition rather than clinical evidence. The product is applied directly to the skin as a roll-on gel formulation.

Patient education

📘 MedlinePlus patient leaflet ↗

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.

💊 What it looks like

Color Yellow

One label can cover several strengths, so colors may be combined — always confirm a loose pill against the dispensed prescription label or a pharmacist.

Where does this data come from?

Physical description (imprint, shape, color, scoring, coating) from this product’s FDA Structured Product Labeling (SPL), mirrored from DailyMed / openFDA.

🧪 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 RFW2ET671P
Hydroxypropyl cellulose is a plant-derived thickening agent made from cellulose. It acts as a binder to hold tablet ingredients together and as a film-former to coat tablets or control how fast the medicine releases.
UNII ND2M416302
Isopropyl alcohol is a clear liquid solvent derived from petroleum. In medicines, it dissolves active ingredients and other components, helps the product flow smoothly, and aids in sterilization during manufacturing.
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.

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

The official label also stateshydroxypropyl cellulose, isopropyl alcohol, purified water

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 system	Per g	Per 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: 50 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

Product	Labeler	Pack	NADAC/unit	TE	Status	Price vs. this
Hevert Trauma Roll-On 3 [hp_X]/mL; 1 [hp_X]/mL; 1 [hp_X]/mL; 1 [hp_X]/mL; 6 [hp_X]/mL; 1 [hp_X]/this 54532-0024-06	Hevert	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

🏛️

2016

On the market since

Apr 2016

📍

2026

Currently FDA-listed

10 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 NDC	Description	Marketing start	Status
54532-0024-05	1 BOTTLE, WITH APPLICATOR in 1 CARTON (54532-0024-5) / 50 mL in 1 BOTTLE, WITH APPLICATOR	2016-04-01	Active
54532-0024-06 You're viewing this	1 BOTTLE, WITH APPLICATOR in 1 CARTON (54532-0024-6) / 10 mL in 1 BOTTLE, WITH APPLICATOR	2016-04-01	Active

Pack size FAQ

What quantity is in NDC 54532-0024-06?

NDC 54532-0024-06 is listed by the FDA — 1 bottle, with applicator in 1 carton / 10 ml in 1 bottle, with applicator.

What NDC number is used to bill for this package of Hevert Trauma Roll-On Arnica Montana Root, Bellis Perennis, Calendula Officinalis Flowering Top, Hamamelis Virginiana Root Bark/Stem Bark, Hypericum Perforatum, Achillea Millefolium Flowering Top, Ruta Graveolens Flowering Top, and Comfrey 3 [hp_X]/mL; 1 [hp_X]/mL; 1 [hp_X]/mL; 1 [hp_X]/mL; 6 [hp_X]/mL; 1 [hp_X]/ Gel?

Bill NDC 54532-0024-06 — the 11-digit billing format is 54532002406. 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

Hevert Trauma Roll-On Arnica Montana Root, Bellis Perennis, Calendula Officinalis Flowering Top, Hamamelis Virginiana Root Bark/Stem Bark, Hypericum Perforatum, Achillea Millefolium Flowering Top, Ruta Graveolens Flowering Top, and Comfrey 3 [hp_X]/mL; 1 [hp_X]/mL; 1 [hp_X]/mL; 1 [hp_X]/mL; 6 [hp_X]/mL; 1 [hp_X]/ GEL 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 54532-0024-6, 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: 54532-0024-06, written without dashes as 54532002406. 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 54532-0024-06, the first segment (54532) is the labeler code FDA assigned to Hevert Arzneimittel GmbH & Co KG; the middle segment (0024) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (06) 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 Hevert Arzneimittel GmbH & Co KG. 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 1 other package presentation of this same product, including 1 bottle (54532-0024-05). 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?

Hevert Arzneimittel GmbH & Co KG 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 33 words ▾

Uses For the temporary relief of minor aches and pains, such as: muscle pain and stiffness bruising and swelling Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated .

⏱️ Dosage and Administration 27 words ▾

Directions For external use only Adults and children over 6 years of age: Apply a thin layer of this product to the affected area 3–4 times daily.

⚠️ Warnings 95 words ▾

Warnings For external use only Do not use if you are allergic to Arnica montana, Calendula officinalis (common marigold) or other plants from the daisy family (Compositae), or to any of the ingredients of this product When using this product avoid contact with eyes or mucous membranes do not apply to wounds, damaged or irritated skin Stop use and ask a doctor if condition persists for more than 3 days or gets worse new symptoms occur Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

📦 Storage and Handling 26 words ▾

Other information Store at 68 to 77 °F, lid closed tightly. Keep away from excessive heat or open flame. To report serious adverse events, call 1-855-387-6466

🧪 Active Ingredient 43 words ▾

Active ingredients Purpose Arnica montana, radix 3X Relief of minor aches and pains Bellis perennis 1X Calendula officinalis 1X Hamamelis virginiana 1X Hypericum perforatum 6X Millefolium 1X Ruta graveolens 4X Symphytum officinale 6X "X" indicates a homeopathic dilution. For more information visit: www.hevertusa.com

🧪 Inactive Ingredients 8 words ▾

Inactive ingredients hydroxypropyl cellulose, isopropyl alcohol, purified water

🎯 Purpose 43 words ▾

Active ingredients Purpose Arnica montana, radix 3X Relief of minor aches and pains Bellis perennis 1X Calendula officinalis 1X Hamamelis virginiana 1X Hypericum perforatum 6X Millefolium 1X Ruta graveolens 4X Symphytum officinale 6X "X" indicates a homeopathic dilution. For more information visit: www.hevertusa.com

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

🔗 Related NDC lookups

🧪 All Arnica Montana Root, Bellis Perennis, Calendula Officinalis Flowering Top, Hamamelis Virginiana Root Bark/Stem Bark, Hypericum Perforatum, Achillea Millefolium Flowering Top, Ruta Graveolens Flowering Top, And Comfrey Root NDCsSame ingredient 🏭 All Hevert labeler NDCsLabeler code 54532