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Large Medicated Pain Relief Patches CAMPHOR, MENTHOL, METHYL SALICYLATE 3.1 g/100g; 6 g/100g; 10 g/100g Patch — NDC 41250-0833-05 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Large Medicated Pain Relief Patches CAMPHOR, MENTHOL, METHYL SALICYLATE 3.1 g/100g; 6 g/100g; 10 g/100g Patch — NDC 41250-833-05 (Billing 41250-0833-05)

by Meijer Distribution Inc · 6 PATCH in 1 BOX / 9 g in 1 PATCH

This is a package of Large Medicated Pain Relief Patches CAMPHOR, MENTHOL, METHYL SALICYLATE 3.1 g/100g; 6 g/100g; 10 g/100g Patch from Meijer Distribution Inc, marketed since Jun 2017 and currently FDA-listed. It is this product's only package size.

NDC 41250-0833-05
🏷️ FDA NDC (as labeled) 41250-833-05 billing pads the product segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 8, 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

NDC database record

One package, one record: these facts belong to NDC 41250-833-05 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
41250 labeler · 833 product · 05 package
Package marketed since
Jun 1, 2017
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 4125083305 6
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 41250-833-05
Product NDC 41250-833
11-digit billing NDC 41250083305
RxCUI 1793147
UNII 5TJD82A1ET, L7T10EIP3A, LAV5U5022Y
Application # M017
SPL Set ID f2928904-a202-414a-b262-287a0a7bda93
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2017-06-01
Route TOPICAL
Dosage form PATCH
Substance CAMPHOR (SYNTHETIC); MENTHOL; METHYL SALICYLATE
Quick answers
  • RxCUI (RxNorm): 1793147
Why two NDCs? The FDA registers this code as 41250-833-05 — 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 → 41250-0833-05. 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 patch containing camphor, menthol, and methyl salicylate, marketed as an over-the-counter monograph product. These three ingredients are commonly used together in pain-relief patches and are typically applied to the skin to create a warming or cooling sensation and to temporarily relieve minor muscle and joint aches. Camphor and menthol work as counterirritants that produce heat or coolness on the skin, while methyl salicylate is also used as a counterirritant in topical pain products. The patch format allows the active ingredients to be absorbed through the skin at the site of discomfort.

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 eachPer 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
41250-0833-05 You're viewing this Main listing 6 PATCH in 1 BOX / 9 g in 1 PATCH 2017-06-01 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Large Medicate Relief Patches 3.1 g/100g; 6 g/100g; 10 g/100g 46122-0645-13 Amerisource 6 patches $0.665 — Availability likely —
Pain Relief Patches 3.1 g/100g; 6 g/100g; 10 g/100g 70000-0368-01 Cardinal 6 patches $0.665 — Availability likely —
Pain Relief Patches 3.1 g/100g; 6 g/100g; 10 g/100g 00363-0907-60 Walgreen 60 patches — — FDA listed —
Walgreens Pain Relieving Patch 100 mg/g; 31 mg/g; 60 mg/g 00363-6716-06 Walgreen 6 patches — — FDA listed —
Large Pain Relieving 3.1 g/100g; 6 g/100g; 10 g/100g 00363-9904-06 Walgreen 6 pouches — — FDA listed —
Pain Relief Medicated 3.1 g/100g; 6 g/100g; 10 g/100g 11822-7883-03 RITE 60 pouches — — FDA listed —
Medicated Pain Relief Patch 3.1 g/100g; 6 g/100g; 10 g/100g 30142-0892-60 Kroger 60 patches — — FDA listed —
Topcare Medicated Pain Relieving Patch 60ct 60 mg/g; 31 mg/g; 100 mg/g 36800-0750-60 Topco 1 pouch — — FDA listed —
Large Medicated Pain Relief Patches 3.1 g/100g; 6 g/100g; 10 g/100gthis 41250-0833-05 Meijer 6 patches — — FDA listed —
Medicated Pain Relief Patches 3.1 g/100g; 6 g/100g; 10 g/100g 41250-0907-60 Meijer 60 patches — — FDA listed —
Pain Relief Patches 3.1 g/100g; 6 g/100g; 10 g/100g 46122-0392-58 Amerisource 40 patches — — Discontinued —
Salonpas 21.56 mg/1; 41.73 mg/1; 69.55 mg 46581-0110-14 Hisamitsu 140 patches — — FDA listed —
Salonpas 86.24 mg/1; 166.92 mg/1; 278.2 mg 46581-0210-06 Hisamitsu 6 patches — — FDA listed —
Pain-Relieving Patch 60 mg/g; 100 mg/g; 31 mg/g 51316-0280-60 CVS 180 patches — — FDA listed —
CVS Health Pain-Relieving Patch 10 g/100g; 3.1 g/100g; 6 g/100g 51316-0992-06 CVS 6 patches — — FDA listed —
Medicated Pain Relief Patches 3.1 g/100g; 6 g/100g; 10 g/100g 53943-0907-60 Discount 60 patches — — FDA listed —
Solstice Pain Relieving 3.1 g/100g; 6 g/100g; 10 g/100g 55614-0210-02 MADISON 2 patches — — FDA listed —
Solstice Pain Relieving 3.1 g/100g; 6 g/100g; 10 g/100g 55614-0310-06 MADISON 6 patches — — FDA listed —
Dollar General Medicated Pain Relief Patch 3.1 g/100g; 6 g/100g; 10 g/100g 55910-0907-20 DOLGENCORP, 20 patches — — FDA listed —
HealthWise 3x Medicated Pain Relief Patch 120 Bulk 10 g/1; 3.1 g/1; 6 g 71101-0032-12 Veridian 120 patches — — FDA listed —
HealthWise 3x Medicated Pain Relief Patch 10 g/1; 3.1 g/1; 6 g 71101-0034-01 Veridian 18 patches — — FDA listed —
TheraCare Medicated Pain Relief 6 g/100g; 3.1 g/100g; 10 g/100g 71101-0128-01 Veridian 60 patches — — FDA listed —
TheraCare Medicated Pain Relief Patches 3.1 g/100g; 6 g/100g; 10 g/100g 71101-0909-06 Veridian 6 patches — — FDA listed —
AsperFlex Advance 86.24 mg/1; 166.92 mg/1; 278.2 mg 71399-4458-06 Akron 6 patches — — FDA listed —
Pain Relief Patches 3.1 g/100g; 6 g/100g; 10 g/100g 72036-0907-60 Harris 60 patches — — FDA listed —
Bonica EaseX Pain Relieving 31 mg/g; 60 mg/g; 100 mg/g 75568-0036-01 Planet 360 patches — — FDA listed —
Careland Pain Relief Plus 31 mg/g; 60 mg/g; 100 mg/g 75568-0039-01 Planet 56 pouches — — FDA listed —
Careland Kinesiology Pain Relieving Tape 31 mg/g; 60 mg/g; 100 mg/g 75568-0049-00 Planet 20 patches — — FDA listed —
Equate Pain Relief Patch Camphor/Menthol/Salicylate 3.1 g/100g; 6 g/100g; 10 g/100g 79903-0039-60 Walmart 60 pouches — — FDA listed —
Equate Medicated Pain Relieving Patch, Large 6-Count 3.1 g/100g; 6 g/100g; 10 g/100g 79903-0308-06 Walmart 6 pouches — — FDA listed —
Sc Herbal .06 g/g; .1 g/g; .031 g/g 82198-0015-01 Big 3 patches — — FDA listed —
Pain Relief Patch 3.1 g/1; 6 g/1; 10 g 83324-0255-60 CDMA, 60 patches — — FDA listed —
Pain 10 g/1001; 3.1 g/1001; 6 g/1001 87255-0005-01 Shenzhen 1 patch — — 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

🏛️
2017
On the market since
Jun 2017
📍
2026
Currently FDA-listed
9 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.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • UNII U333RI6EB7
    Hydrogenated polydecene type I is a synthetic oil derived from plant-based polymers. It acts as a lubricant and glidant to help powder ingredients flow smoothly during tablet or capsule manufacturing.
  • UNII 6ZAE7X688J
    A refined mineral oil derived from crude petroleum. It serves as a lubricant and binder in tablet and capsule formulations, helping medicines slide smoothly through manufacturing equipment and improving how ingredients stick together.
  • UNII 255PIF62MS
    A synthetic antioxidant compound used to prevent oils and fats in medications from breaking down or becoming rancid during storage. It helps maintain the medicine's stability and shelf life.
  • UNII 5Z4DPO246A
    A synthetic plastic polymer made from styrene and acrylamide monomers. It acts as a film-former and binder in tablets and capsules, helping hold ingredients together and control how quickly the medicine dissolves and releases in your body.

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

The official label also statesHydrogenated Poly, Pentaerythrityl Tetra-di-t-butyl Hydroxyhydrocinnamate, Petroleum, Styrene / Isoprene Copolymer

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

LabelerMeijer Distribution Inc
FDA applicationM017 (OTC MONOGRAPH DRUG)
Labeler code41250
First marketedJun 2017
Product typeHuman Otc Drug
Portfolio245 products on file

More NDCs from Meijer Distribution Inc labeler code 41250

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 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 11 words ▾

Indication and Usage For temporary relief of minor aches and pains.

⏱️ Dosage and Administration 72 words ▾

Directions Adults and children 12 years of age and over: Clean and dry affected area. Remove patch from film, apply to affected area not more than 3 to 4 times daily. Remove patch from the skin after at most, 8-hour application.

Children under 12 years of age: consult physician. Inactive Ingredients Hydrogenated Poly, Pentaerythrityl Tetra-di-t-butyl Hydroxyhydrocinnamate, Petroleum, Styrene / Isoprene Copolymer Indication and Usage For temporary relief of minor aches and pains.

⚠️ Warnings 20 words ▾

For External Use Only Allergy alert: If prone to allergic reaction from asprin or salicylates, consult a doctor before use

🧪 Active Ingredient 18 words ▾

Active Ingredients Active Ingredients Purpose Camphor 3.1% ......................Topical Analgesic Menthol 6.0% .......................Topical Analgesic Methyl Salicylate 10.0% .......Topical Analgesic

🧪 Inactive Ingredients 12 words ▾

Inactive Ingredients Hydrogenated Poly, Pentaerythrityl Tetra-di-t-butyl Hydroxyhydrocinnamate, Petroleum, Styrene / Isoprene Copolymer

🎯 Purpose 22 words ▾

Uses For temporary relief of minor aches and pains of muscles and joints associated with arthritis, simple backache, strains, sprains, and bruises.

📄 Do Not Use 22 words ▾

Do not use: On wounds or damaged skin With a heating pad If you are allergic to any ingredients of this product

📄 When Using This Product 68 words ▾

When using this product Use only as directed Avoid contact with eyes, mucous membranes or rashes Do not bandage tighly Do not use at the same time as other topical analgesics Dispose of used patch in manner that keeps product away from childrens and pets. Used patches still contain the drug product that can produce serious adverse effects if a child or pet chews or ingests this patch.

📄 Stop Use and Ask a Doctor If 34 words ▾

Stop use and consult a doctor If rash, itching or excessive skin irritation develops If condition worsens if symptoms last more than 7 days or clear up and occur again with a few days

📄 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 6 words ▾

Questions or Comments Call toll-free 1-866-326-1313

📄 Package Label / Principal Display Panel 33 words ▾

Pain Relief Patch Label Other Information : Store in clean, dy place outside of direct sunlight. Protect from excessive moisture. DIST. BY MEIJER DISTRIBUTION, INC. GRAND RAPIDS, MI 49544 www.meijer.com Box of 60

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 CAMPHOR, MENTHOL, METHYL SALICYLATE — the ingredient across all brands.

Top reported reactions

Application Site Burn6
Application Site Pain6
Chemical Injury4
Erythema3
Malaise3
Pain3
Rash3

Age at onset

Adult1

Reporter sex

49 reports
Male · 34%
Female · 66%

Serious outcomes

Hospitalization9
Life-threatening1
Disabling1
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 4 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
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 "Otc Monograph Drug". 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 Meijer Distribution Inc. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Meijer Distribution 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.
← 41250-0831-43 · Meijer, 41250-0834-05 · Meijer →
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.