NDC 62795-7005-06 — T-Relief ACONITUM NAPELLUS, ARNICA MONTANA

🆔 Identity & classification

FDA NDC (as labeled) 62795-7005-6

Product NDC 62795-7005

11-digit billing NDC 62795700506

NCPDP billing unit GM — per gram (weight)

UNII U0NQ8555JD, O80TY208ZW, 5EF0HWI5WU, WQZ3G9PF0H, 2HU33I03UY, 18E7415PXQ +7 more

SPL Set ID edb2fe62-e990-4cef-8600-9d1b85bffa5a

DEA schedule Non-controlled

Marketing category UNAPPROVED HOMEOPATHIC

Marketing status On market

FDA listing status Listed (active directory)

Marketing start 2016-07-31

Route TOPICAL

Dosage form GEL

Substance ACONITUM NAPELLUS; ARNICA MONTANA; BAPTISIA TINCTORIA ROOT; ATROPA BELLADONNA; BELLIS PERENNIS; CALENDULA OFFICINALIS FLOWERING TOP; MATRICARIA RECUTITA; ECHINACEA, UNSPECIFIED; HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; HYPERICUM PERFORATUM; ACHILLEA MILL

GPI-14 99870010004000

GPI class T-Relief Pain Relief

Why two NDCs? The FDA registers this code as 62795-7005-6 — 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 → 62795-7005-06. 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

LabelerMediNatura Inc

Labeler code62795

First marketedJul 2016

Product typeHuman Otc Drug

Portfolio33 products on file

🔎 All NDCs from MediNatura Inc

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?

T-Relief is a topical gel marketed as a homeopathic product. It contains multiple plant-derived ingredients including arnica, calendula, echinacea, hypericum, hamamelis, and comfrey, which are traditionally used in homeopathic practice for minor discomfort and skin concerns. Homeopathic products are based on traditional use rather than FDA evaluation for effectiveness. This product is not approved by the FDA and is marketed under homeopathic regulations.

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.

🧪 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 3K9958V90M
A liquid solvent derived from fermentation or chemical synthesis. In medicines, alcohol dissolves active ingredients, helps preserve the product, and improves how the body absorbs certain drugs.
UNII 4Q93RCW27E
A synthetic polymer made from acrylic acid that's crosslinked for stability. It acts as a thickener and gelling agent in creams and gels, helping the medicine spread evenly and maintain its texture.
UNII HIE492ZZ3T
Phenoxyethanol is a synthetic preservative and antimicrobial agent used to prevent bacterial and fungal growth in medicines and cosmetic products, extending shelf life and maintaining product safety.
UNII 55X04QC32I
A strong alkaline chemical used to adjust and maintain the pH balance of liquid medicines. It helps keep the medicine stable and ensures it stays effective during storage.
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.

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

The official label also statesCarbomer 980, Phenoxyethanol, Purified Water, SD Alcohol 3C, Sodium Hydroxide.

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: 250 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

Product	Labeler	Pack	NADAC/unit	TE	Status	Price vs. this
T-Relief 1 [hp_X]/g; 1 [hp_X]/g; 4 [hp_X]/g; 2 [hp_X]/g; 2 [hp_X]/g; 1 [hp_X]/g; 2 [hp_X]/g; 1this 62795-7005-06	MediNatura	1 tube	—	—	FDA listed	—
T-Relief Extra Strength Gel 1 [hp_X]/g; 1 [hp_X]/g; 4 [hp_X]/g; 2 [hp_X]/g; 2 [hp_X]/g; 1 [hp_X]/g; 2 [hp_X]/g; 1 62795-7006-04	MediNatura	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

🏛️

2016

On the market since

Jul 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.

🔬 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 T-Relief (this brand).

Top reported reactions

Hot Flush3

Asthenia2

Diarrhoea2

Pain2

Vomiting2

Abnormal Behaviour1

Arthritis1

Age at onset

Adult1

Reporter sex

Male · 20%

Female · 80%

Serious outcomes

Hospitalization2

Life-threatening1

Disabling1

Reports over time (by year) — tap or hover for the count & year

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.

📦 Packaging — all sizes for this product

Package NDC	Description	Marketing start	Status
62795-7005-05	250 g in 1 BOTTLE (62795-7005-5)	2016-07-31	Active
62795-7005-06 You're viewing this	1 TUBE in 1 CARTON (62795-7005-6) / 57 g in 1 TUBE	2016-07-31	Active

Pack size FAQ

What quantity is in NDC 62795-7005-06?

NDC 62795-7005-06 is listed by the FDA — 1 tube in 1 carton / 57 g in 1 tube.

What NDC number is used to bill for this package of T-Relief ACONITUM NAPELLUS, ARNICA MONTANA, BAPTISIA TINCTORIA ROOT, ATROPA BELLADONNA, BELLIS PERENNIS, CALENDULA OFFICINALIS FLOWERING TOP, MATRICARIA RECUTITA, ECHINACEA UNSPECIFIED, HAMAMELIS VIRGINIANA ROOT BARK STEM BARK, HYPERICUM PERFORATUM, ACHILLEA MILLE 1 [hp_X]/g; 1 [hp_X]/g; 4 [hp_X]/g; 2 [hp_X]/g; 2 [hp_X]/g; 1 [hp_X]/g; 2 [hp_X]/g; 1 Gel?

Bill NDC 62795-7005-06 — the 11-digit billing format is 62795700506. 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

T-Relief ACONITUM NAPELLUS, ARNICA MONTANA, BAPTISIA TINCTORIA ROOT, ATROPA BELLADONNA, BELLIS PERENNIS, CALENDULA OFFICINALIS FLOWERING TOP, MATRICARIA RECUTITA, ECHINACEA UNSPECIFIED, HAMAMELIS VIRGINIANA ROOT BARK STEM BARK, HYPERICUM PERFORATUM, ACHILLEA MILLE 1 [hp_X]/g; 1 [hp_X]/g; 4 [hp_X]/g; 2 [hp_X]/g; 2 [hp_X]/g; 1 [hp_X]/g; 2 [hp_X]/g; 1 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 62795-7005-6, 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: 62795-7005-06, written without dashes as 62795700506. 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 62795-7005-06, the first segment (62795) is the labeler code FDA assigned to MediNatura Inc; the middle segment (7005) 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 MediNatura Inc. 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 250 g (62795-7005-05). 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?

MediNatura Inc 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 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose

🎯 Indications and Usage 12 words ▾

INDICATIONS Relieves • Joint Pain • Back Pain •Muscular Pain •Nerve Pain

⏱️ Dosage and Administration 54 words ▾

DIRECTIONS Twist off cap and remove the foil seal. Adults and children 4 years and older: Apply generously to affected areas 2 to 3 times daily, or more often if necessary. Massage thoroughly into the skin. If appropriate, mild compression or occlusive bandaging may be applied. For children under 4, consult your health professional.

⚠️ Warnings 82 words ▾

WARNINGS For external use only. Do not apply over open wounds or broken skin. If symptoms persist or worsen, or if a rash develops, a health professional should be consulted.

In rare cases, allergic skin reactions may develop. Do not use if known sensitivity to T-Relief TM or any of its ingredients exists. Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away. If pregnant or breast-feeding, ask a health professional before use.

🧪 Active Ingredient 102 words ▾

ACTIVE INGREDIENTS Active ingredients Purpose *Aconitum napellus 1X 0.5%................Reduces joint and back pain *Arnica montana 1X 2%........Reduces joint and back pain *Arnica montana 3X 2%..........Reduces joint and back pain *Arnica montana10X 2%........Reduces joint and back pain *Baptisia tinctoria 4X 1% ..................Reduces joint and muscle pain *Belladonna 2X 1%...........................Reduces back pain *Bellis perennis 2X 1%......................Relieves joint and muscle soreness *Calendula officinalis 1X 1%..............Relieves pain *Chamomilla 2X 1%.........................Soothing pain relief *Echinacea 1X 1%............................Relieves pain *Hamamelis virginiana 2X 2%...........Relieves joint and muscle soreness *Hypericum perforatum 6X 0.1%.........Relieves pain *Millefolium 2X 2%...........................Relieves pain *Ruta graveolens 4X 2%..................Relieves pain *Symphytum officinale 4X 0.1%..........Relieves joint pain *Natural Ingredients

🧪 Inactive Ingredients 12 words ▾

INACTIVE INGREDIENTS Carbomer 980, Phenoxyethanol, Purified Water, SD Alcohol 3C, Sodium Hydroxide.

🎯 Purpose 18 words ▾

USES For the temporary relief of minor: Joint Pain • Back Pain • Muscular Pain • Nerve Pain

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

🔗 Related NDC lookups

🧪 All Aconitum Napellus, Arnica Montana, Baptisia Tinctoria Root, Atropa Belladonna, Bellis Perennis, Calendula Officinalis Flowering Top, Matricaria Recutita, Echinacea Unspecified, Hamamelis Virginiana Root Bark Stem Bark, Hypericum Perforatum, Achillea Mille NDCsSame ingredient 🏭 All MediNatura labeler NDCsLabeler code 62795