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Tagrid Arnica Bruise Arnica Montana 1X HPUS (7%) 7 mg/100g Cream, 100 g — NDC 85384-0015-03 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Tagrid Arnica Bruise Arnica Montana 1X HPUS (7%) 7 mg/100g Cream, 100 g — NDC 85384-0015-3 (Billing 85384-0015-03)

by TAGRID LLC · 100 g in 1 JAR

This is a package of 100 g of Tagrid Arnica Bruise Arnica Montana 1X HPUS (7%) 7 mg/100g Cream from TAGRID LLC, marketed since Jul 2025 and currently FDA-listed.

NDC 85384-0015-03
🏷️ FDA NDC (as labeled) 85384-0015-3 billing pads the package segment with a zero
This package
Contains100 g Pack sizes4 compare ↓
Product page 85384-0015-01 Also comes in: 96 g 85384-0015-4 120 g 85384-0015-1 120 g 85384-0015-2
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 8, 2026 · this listing last changed Oct 8, 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

NDC database record

One package, one record: these facts belong to NDC 85384-0015-3 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
85384 labeler · 0015 product · 3 package
Package marketed since
Jul 19, 2025
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC-A, from the NDC)
3 8538400153 0
FDA record last changed
Oct 8, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 85384-0015-3
Product NDC 85384-0015
11-digit billing NDC 85384001503
SPL Set ID 0174092f-e10f-4c93-a677-facbdcf1a6ea
DEA schedule Non-controlled
Marketing category UNAPPROVED HOMEOPATHIC
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2025-07-19
Route TOPICAL
Dosage form CREAM
Substance ARNICA MONTANA
Why two NDCs? The FDA registers this code as 85384-0015-3 — 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 → 85384-0015-03. 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.

Clinical

🧪 What is this product?

Tagrid Arnica Bruise is a topical cream containing arnica montana at a 1X homeopathic potency. This is an unapproved homeopathic product marketed based on traditional homeopathic use rather than FDA-evaluated effectiveness. In homeopathic practice, arnica montana is traditionally used for minor bruising and related skin concerns. Homeopathic products are not evaluated by the FDA for safety or effectiveness in the same way as conventional medications.

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.

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: 96 g 120 g 120 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.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
85384-0015-01 85384-0015-1 Main listing 120 g in 1 TUBE 2025-07-19 — Active
85384-0015-02 85384-0015-2 120 g in 1 JAR 2025-07-19 — Active
85384-0015-03 You're viewing this 100 g in 1 JAR 2025-07-19 — Active
85384-0015-04 85384-0015-4 96 g in 1 JAR 2025-07-19 — Active

Pack size FAQ

What quantity is in this package?
This package contains 100 g — 100 g in 1 jar.
How does this package differ from NDC 85384-0015-04?
Both are Tagrid Arnica Bruise Arnica Montana 1X HPUS (7%) 7 mg/100g Cream — the drug itself is identical. This page's package is the 100 g one, while NDC 85384-0015-04 is the 96 g package.
What NDC number is used to bill for this package of Tagrid Arnica Bruise Arnica Montana 1X HPUS (7%) 7 mg/100g Cream?
Use the 11-digit billing form listed in the identifiers section of this page. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Tagrid DMSO Cream Arnica Montana 1X HPUS (7%) 7 mg/100g 85384-0020-01 TAGRID 114 g — — FDA listed —
Dr.Johnes Arnica Bruise Arnica Montana 1X HPUS (7%) 7 mg/100g 85818-0006-01 Dr.Johnes 100 g — — FDA listed —
Tagrid Arnica Bruise Arnica Montana 1X HPUS (7%) 7 mg/100g 85818-0005-01 Dr.Johnes 100 g — — FDA listed —
Tagrid Arnica Bruise Arnica Montana 1X HPUS (7%) 7 mg/100gthis 85384-0015-03 TAGRID 100 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
Jul 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.

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 344S277G0Z
    Allantoin is a naturally derived compound that helps soften and soothe skin. In medicines, it works as a skin-conditioning agent and may help support wound healing and reduce irritation in topical formulations.
  • 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 P0M7O4Y7YD
    A plant extract from calendula flowers, traditionally used in formulations. It typically serves as a botanical ingredient that may provide color, fragrance, or skin-conditioning properties to topical products.
  • UNII 4YS74Q4G4J
    A plant extract from Centella asiatica containing natural compounds called triterpenoids. It's used as an active ingredient in some formulations for its purported skin-supporting properties, though it functions as a botanical additive rather than a structural component of the medicine.
  • UNII Q9L0O73W7L
    Coconut oil is a natural fat extracted from coconut fruit. It's used in medicines as a lubricant, emollient, or carrier to help dissolve or deliver active ingredients smoothly through the formulation.
  • UNII RUU8G67GQM
    Escin is a natural mixture of plant compounds extracted from horse chestnut seeds. It acts as a surfactant and emulsifier in medicines, helping to dissolve and mix ingredients that normally don't blend well together.
  • UNII A034SE7857
    Phytonadione is a form of vitamin K, a naturally occurring compound. It's used in medicines as an active pharmaceutical ingredient to support blood clotting, though it may also serve as a colorant or stabilizer in some formulations.
  • UNII M6S840WXG5
    Purslane is a plant-derived ingredient used in pharmaceuticals as a natural source of beneficial compounds. It functions as an antioxidant and anti-inflammatory agent to help stabilize the formula and support product shelf life.
  • UNII K49155WL9Y
    Shea butter is a fat extracted from shea tree nuts. It's used in medicines as an emollient and lubricant to soften the product, improve texture, and help ingredients blend smoothly together.
  • UNII 9LBV3F07AZ
    A synthetic, oil-soluble form of vitamin C used as an antioxidant to prevent degradation of the medicine and maintain its stability during storage.
  • UNII R0ZB2556P8
    Tocopherol is a form of vitamin E derived from plant oils. It acts as an antioxidant in medicines to prevent oils and fats from breaking down and spoiling 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.

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

The official label also statesInactive ingredients: Purified Water Butyrospermum Parkii (Shea Butter) Tocopherol (Vitamin E) Tetrahexyldecyl Ascorbate (Vitamin C) Allantoin Aloe Barbadensis Leaf Juice Calendula Officinalis Flower Extract Centella Asiatica Extract Portulaca Oleracea Extract Cocos Nucifera (Coconut) Oil Phytonadione (Vitamin K) Escin

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.

Manufacturer & labeler

LabelerTAGRID LLC
Labeler code85384
First marketedJul 2025
Product typeHuman Otc Drug
Portfolio26 products on file

More NDCs from TAGRID LLC labeler code 85384

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.

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 📄 Do Not Use 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 🤰 If Pregnant or Breast-Feeding 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 16 words ▾

Uses: Temporarily relieves pain, swelling, and discoloration associated with: Bruises Minor falls Sports injuries Muscle soreness

⏱️ Dosage and Administration 26 words ▾

Directions: Apply a thin layer to the affected area 2 to 3 times daily. Gently massage until absorbed. Use as soon as possible after minor injury.

⚠️ Warnings 80 words ▾

For external use only Do not apply to broken skin or open wounds. Avoid contact with eyes. When using this product Avoid contact with eyes. Stop use and ask a doctor if Condition worsens Symptoms persist for more than 7 days or clear up and occur again within a few days. If pregnant or breast-feeding Ask a health professional before use Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

🧪 Active Ingredient 7 words ▾

Active ingredient: Arnica Montana 1X HPUS (7%)

🧪 Inactive Ingredients 38 words ▾

Inactive ingredients: Purified Water Butyrospermum Parkii (Shea Butter) Tocopherol (Vitamin E) Tetrahexyldecyl Ascorbate (Vitamin C) Allantoin Aloe Barbadensis Leaf Juice Calendula Officinalis Flower Extract Centella Asiatica Extract Portulaca Oleracea Extract Cocos Nucifera (Coconut) Oil Phytonadione (Vitamin K) Escin

🎯 Purpose 18 words ▾

Purpuse:Bruise Relief. "HPUS" indicates that this ingredient is officially monographed in the Homeopathic Pharmacopoeia of the United States.

📄 Do Not Use 13 words ▾

Do not apply to broken skin or open wounds. Avoid contact with eyes.

📄 When Using This Product 8 words ▾

When using this product Avoid contact with eyes.

📄 Stop Use and Ask a Doctor If 26 words ▾

Stop use and ask a doctor if Condition worsens Symptoms persist for more than 7 days or clear up and occur again within a few days.

🤰 If Pregnant or Breast-Feeding 10 words ▾

If pregnant or breast-feeding Ask a health professional before use

📄 Keep Out of Reach of Children 19 words ▾

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

📄 Questions or Comments 7 words ▾

Questions or comments? Contact us at [email protected]

📄 Package Label / Principal Display Panel 9 words ▾

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL arnica.jpg arnica-jar arnica-can arnica-can ARNICA-can-label

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

About this NDC listing & data coverage

Over-the-counter (OTC) product Homeopathic listing

About homeopathic listings

Tagrid Arnica Bruise Arnica Montana 1X HPUS (7%) 7 mg/100g 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 form printed on the packaging and shown on DailyMed is the one the FDA registered. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero and the dashes are dropped. The Identity section at the top of this page lists each form of this code.
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 TAGRID LLC. 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 3 other package presentations of this same product, including 96 g (85384-0015-04), 120 g (85384-0015-01), 120 g (85384-0015-02). 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?
TAGRID LLC 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.
← 85384-0014-01 · TAGRID 85384-0016-01 · TAGRID →
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.