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Equate Arnica Pain Relieving ARNICA MONTANA WHOLE 70 mg/g Gel — NDC 49035-673-01 (Billing 49035-0673-01)

by Wal-Mart Stores, Inc. · 1 CYLINDER in 1 CARTON / 74 g in 1 CYLINDER

This is a package of Equate Arnica Pain Relieving ARNICA MONTANA WHOLE 70 mg/g Gel from Wal-Mart Stores, Inc., marketed since Apr 2020 and currently FDA-listed. It is this product's only package size.

NDC 49035-0673-01
🏷️ FDA NDC (as labeled) 49035-673-01 billing pads the product segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed 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

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 49035-673-01
Product NDC 49035-673
11-digit billing NDC 49035067301
UNII O80TY208ZW
UPC 0687737352406
SPL Set ID 731d2345-8ad0-431d-aa5c-ac426517ae4b
DEA schedule Non-controlled
Marketing category UNAPPROVED HOMEOPATHIC
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2020-04-30
Route TOPICAL
Dosage form GEL
Substance ARNICA MONTANA WHOLE
Why two NDCs? The FDA registers this code as 49035-673-01 — 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 → 49035-0673-01. 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.

Clinical

🧪 What is this product?

This is a topical gel containing arnica montana whole, marketed as a homeopathic product. In homeopathic practice, arnica is traditionally used to address minor pain and bruising, though homeopathic products are not evaluated by the FDA for effectiveness. This product is formulated for application directly to the skin and is sold over the counter based on homeopathic tradition rather than proven clinical 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.

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.
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
49035-0673-01 You're viewing this Main listing 1 CYLINDER in 1 CARTON / 74 g in 1 CYLINDER 2020-04-30 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Equate Arnica Pain Relieving 70 mg/gthis 49035-0673-01 Wal-Mart 1 cylinder — — 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

🏛️
2020
On the market since
Apr 2020
📍
2026
Currently FDA-listed
6 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.

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.

Loading inactive ingredients from the official FDA label in the background. No external source is being called by this page request.
Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.

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

LabelerWal-Mart Stores, Inc.
Labeler code49035
First marketedApr 2020
Product typeHuman Otc Drug
Portfolio83 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.

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 📄 When Using This Product 🤰 If Pregnant or Breast-Feeding 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 28 words ▾

Uses** According to homeopathic principles, the active ingredient in this product temporarily relieves minor symptoms such as: bruising and swelling sprains backaches muscular aches and pains strains stiffness

⏱️ Dosage and Administration 33 words ▾

Directions For adults and children 2 years of age and older: Apply a thin layer to affected area as soon as possible after minor injury. Repeat 3 times a day or as needed.

⚠️ Warnings 198 words ▾

Warnings For external use only. Do not use on damaged skin, open wounds, or mucous membranes. Test on a small patch of skin before applying generously.

According to homeopathic principles, symptoms may temporarily worsen before improving (Initial exacerbation of symptoms). Avoid contact with eyes. Do not use if you are allergic to Arnica montana (Asteracea flower) or any of this product's inactive ingredients.

Do not bandage tightly or use with a heating pad. Do not use with heating pads or other heating devices. If conditions worsen or if symptoms persist for more than 72 hours or clear up and occur again within a few days, discontinue use of this product and consult a physician.

When using this product use only as directed avoid contact with eyes and mucous membranes if redness is present, discontinue use and consult a doctor if skin irritation occurs, discontinue use a transient burning sensation may occur upon application but generally disappears in several days. Flammable keep away from fire or flame If pregnant, trying to get 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 immediately.

📦 Storage and Handling 14 words ▾

Other information Active ingredients are manufactured according to homeopathic principles. Store at room temperature

🧪 Active Ingredient 25 words ▾

Active ingredient‡ Arnica Montana 1X HPUS 7% The letters HPUS indicate that this ingredient is officially included in the Homeopathic Pharmacopoeia of the United States.

🧪 Inactive Ingredients 10 words ▾

Inactive ingredients alcohol denat., capsaicin, carbomer, glycerin, sodium hydroxide, water.

🎯 Purpose 12 words ▾

Purpose** Relieve muscle pain and stiffness, swelling from injuries, discoloration from bruises

📄 When Using This Product 45 words ▾

When using this product use only as directed avoid contact with eyes and mucous membranes if redness is present, discontinue use and consult a doctor if skin irritation occurs, discontinue use a transient burning sensation may occur upon application but generally disappears in several days.

🤰 If Pregnant or Breast-Feeding 14 words ▾

If pregnant, trying to get pregnant or breast-feeding, ask a health professional before use.

📄 Keep Out of Reach of Children 18 words ▾

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

📄 Questions or Comments 4 words ▾

Questions or comments? 1-888-287-1915

📄 Package Label / Principal Display Panel 72 words ▾

PRINCIPAL DISPLAY PANEL - 74 g Cylinder Carton NDC 49035-673-01 equate™ Compare to Arnicare® Gel active ingredient* with Capsaicin Arnica Pain Relieving † ** Gel Homeopathic Medicine Relieves: † ** Muscle pain & stiffness Swelling from injuries Bruising Non-greasy Fast-absorbing Unscented Paraben-free No Mess Roll-On Applicator NET WT

2.6OZ (74g) **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. PRINCIPAL DISPLAY PANEL - 74 g Cylinder Carton

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

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 ARNICA MONTANA WHOLE — the ingredient across all brands.

Top reported reactions

Diarrhoea3
Hot Flush3
Abdominal Distension2
Asthenia2
Dehydration2
Fatigue2
Gait Disturbance2

Age at onset

Adult2
Elderly1

Reporter sex

15 reports
Male · 25%
Female · 75%

Serious outcomes

Hospitalization4
Life-threatening1
Disabling1
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 3 0
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.

About this NDC listing & data coverage

Over-the-counter (OTC) product Homeopathic listing

About homeopathic listings

Equate Arnica Pain Relieving ARNICA MONTANA WHOLE 70 mg/g 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 — Not published for this NDC No photo available yet for this listing.
Inactive ingredients (structured) — Not published for this NDC The labeler did not submit a structured excipient list, or no SPL is 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 Wal-Mart Stores, Inc.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Wal-Mart Stores, 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.
← 49035-0672-51 · Wal-Mart 49035-0674-16 · WAL-MART →
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.