CVS Muscle Balm and Roll-On Camphor, Menthol Kit
by CVS Pharmacy · 1 KIT in 1 CARTON (51316-241-01) * 74 mL in 1 BOTTLE, WITH APPLICATOR (51316-244-25) * 18 g in 1 JAR (51316-243-63)
NDC 51316-0241-01
🏷️ FDA NDC (as labeled)
51316-241-01
billing pads the product segment with a zero
OTC
On market
Non-controlled
🗂️ Data synced Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →
🆔 Identity & classification
FDA NDC (as labeled)
51316-241-01
Product NDC
51316-241
11-digit billing NDC
51316024101
RxCUI
1089847
Application #
M017
SPL Set ID
4e40025a-070a-508e-e063-6394a90af5d7
DEA schedule
Non-controlled
Marketing category
OTC MONOGRAPH DRUG
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
2026-04-13
Route
TOPICAL
Dosage form
KIT
Why two NDCs?
The FDA registers this code as 51316-241-01 — 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 → 51316-0241-01. 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.
🏭 Manufacturer & labeler
LabelerCVS Pharmacy
FDA applicationM017 (OTC MONOGRAPH DRUG)
Labeler code51316
First marketedApr 2026
Product typeHuman Otc Drug
Portfolio550 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.
🩺 Clinical
🧪 What is this product?
This CVS kit contains a muscle balm and roll-on product with camphor and menthol as active ingredients. Both are topical ingredients commonly used to produce a warming or cooling sensation on the skin and are typical components in over-the-counter products meant for temporary relief of minor muscle discomfort. This is an OTC monograph drug, meaning it is marketed under FDA's established rules for this category of product rather than through an individual drug application.
Patient education
Supplement & herbal interactions
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.
💬 Questions about Camphor, Menthol?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
🧪 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.
From the label’s inactive-ingredient sectionCinnamomum Cassia Leaf Oil, Eugenia Caryophyllus Bud Oil, Melaleuca Leucadendron Cajuputi Leaf Oil, Mentha Arvensis Leaf Oil, Paraffin, Petrolatum Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Cinnamomum Cassia Leaf Oil, Eugenia Caryophyllus Bud Oil, Melaleuca Leucadendron Cajuputi Leaf Oil, Mentha Arvensis Leaf Oil, SD Alcohol 40-B, Water
This is label-wide narrative text, not a normalized exact-product ingredient list. A label can cover multiple strengths or packages.
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.
💲 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 each | 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.
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 |
|---|---|---|---|---|---|---|
| Leader Anti-Itch .5 g/100g; .5 g/100g 70000-0546-01 | LEADER/Cardinal | 212 g | $0.022 | — | Availability likely | — |
| GNP Anti Itch .5 g/100g; .5 g/100g 46122-0573-10 | AMERISOURCEBERGEN | 212 g | $0.022 | — | Availability likely | — |
| Rugby Anti-Itch .5 g/100g; .5 g/100g 00536-1268-12 | RUGBY | 212 g | $0.022 | — | Availability likely | — |
| CVS Muscle Balm 110 mg/g; 110 mg/g 51316-0240-01 | CVS | 1 jar | — | — | FDA listed | — |
| CVS Muscle Balm and Roll-Onthis 51316-0241-01 | CVS | 1 kit | — | — | FDA listed | — |
| Tiger Balm Ultra Strength 110 mg/g; 110 mg/g 66761-0315-02 | Haw | 2 g | — | — | FDA listed | — |
| Muscle Balm 110 mg/g; 110 mg/g 66902-0142-63 | Natural | 18 g | — | — | FDA listed | — |
| GuruNanda Pain Relief 110 mg/g; 110 mg/g 70708-0937-13 | GURUNANDA, | 1 jar | — | — | FDA listed | — |
| Ultra Strength Pain Relief Balm 110 mg/g; 110 mg/g 73492-0711-18 | ALAINA | 1 bottle | — | — | FDA listed | — |
| Pain Relief Balm 110 mg/g; 110 mg/g 73492-0718-15 | ALAINA | 1 jar | — | — | FDA listed | — |
| Equate Pain Relief Balm 110 mg/g; 110 mg/g 79903-0105-18 | WALMART, | 1 bottle | — | — | FDA listed | — |
| Ultra-Strength Pain Relief Analgesic 110 mg/g; 110 mg/g 82442-0311-01 | TARGET | 1 jar | — | — | FDA listed | — |
| Ay Bendito - Thermoactive 6 g/100g; 4 g/100g 72524-0641-04 | AY | 113 g | — | — | FDA listed | — |
| CBD Clinic Deep-Rub Pain Relief - Level 5 5 g/100g; 15 g/100g 73096-0754-28 | ABACUS | 287.55 g | — | — | FDA listed | — |
| Active Recovery Pain Relief 16 g/100g; 11 g/100g 79845-0768-44 | Charlotte's | 44 g | — | — | FDA listed | — |
| Dragon Pain Relieving 10 g/100g; 11 g/100g 83552-0119-00 | AMERICANNA | 1 tube | — | — | FDA listed | — |
| Eagle Brand Medicated Roll On Refresh 2.2 g/100mL; 14 g/100mL 43405-0012-08 | Borden | 1 bottle | — | — | FDA listed | — |
| XtraCare Vaporizing Chest Rub 5 g/113g; 1 g/113g 57337-0051-01 | Rejoice | 113 g | — | — | FDA listed | — |
| Eagle Brand Medicated Oil Refresh 14 g/100mL; 2.2 g/100mL 60954-0013-24 | PT. | 1 bottle | — | — | FDA listed | — |
| Dragon Pain Relieving Balm 11 g/100g; 15 g/100g 83552-0125-00 | Americanna | 14 g | — | — | FDA listed | — |
| Vicks VapoFreeze PAIN RELIEVING .16 g/g; .036 g/g 84126-0302-03 | The | 1 tube | — | — | FDA listed | — |
| Core Relief 3 g/100mL; 5 g/100mL 87179-0053-02 | Copper | 59 ml | — | — | FDA listed | — |
| Mentholatum Original 90 mg/g; 13 mg/g 10742-0002-01 | The | 1 jar | — | — | FDA listed | — |
| Dragon Pain Relieving Balm 5.3 g/100g; 3.1 g/100g 83552-0105-00 | Americanna | 96.4 g | — | — | FDA listed | — |
| Dragon Pain Relieving 10 g/100g; 11 g/100g 83552-0120-00 | AMERICANNA | 479 g | — | — | FDA listed | — |
| Dragon Pain Relieving Balm 11 g/100g; 15 g/100g 83552-0123-00 | Americanna | 1 jar | — | — | FDA listed | — |
| HERSTAT PLUS Cold Sore Treatment 3 g/100g; .1 g/100g 90100-0221-02 | Herstat | 1 tube | — | — | FDA listed | — |
| terrasil Bruise and Pain Relief Maximum Strength 16 g/100g; 11 g/100g 24909-0042-50 | Aidance | 50 g | — | — | FDA listed | — |
| Ay Bendito - Thermoactive 6 g/100g; 4 g/100g 72524-0005-06 | AY | 5 g | — | — | FDA listed | — |
| Dragon Pain Relieving Balm 5.3 g/100g; 3.1 g/100g 83552-0101-00 | Americanna | 1 jar | — | — | FDA listed | — |
| Dragon Pain Relieving Balm 10 g/100g; 11 g/100g 83552-0111-00 | AMERICANNA | 1 jar | — | — | FDA listed | — |
| Dragon Pain Relieving 3.1 g/100g; 5.3 g/100g 83552-0118-00 | AMERICANNA | 1 tube | — | — | FDA listed | — |
| Dragon Pain Relieving Balm 11 g/100g; 15 g/100g 83552-0121-00 | Americanna | 96.4 g | — | — | FDA listed | — |
| Paingel Unguento 11 g/100g; 16 g/100g 85110-0116-04 | NACOR | 113 g | — | — | FDA listed | — |
| Softlips Naturals Medicated Elderberry Acai 5 mg/g; 10 mg/g 10742-8482-01 | The | 2 tubes | — | — | FDA listed | — |
| MYCO Clinic Pain Relief 11 g/100g; 16 g/100g 24909-0012-50 | Aidance | 50 g | — | — | FDA listed | — |
| Rhuli Gel .3 g/100g; .3 g/100g 69396-0031-20 | Trifecta | 1 tube | — | — | FDA listed | — |
| Professional Therapy MuscleCare Pro Pain Relieving Cold Gel 4 g/100g; 10 g/100g 70039-0302-16 | ACTIVE | 453 g | — | — | FDA listed | — |
| Ay Bendito - Thermoactive 6 g/100g; 4 g/100g 72524-0010-03 | AY | 90 g | — | — | FDA listed | — |
| Dragon Pain Relieving Balm 10 g/100g; 11 g/100g 83552-0117-00 | AMERICANNA | 14 g | — | — | FDA listed | — |
| Eagle Brand Medicated Roll On Refresh 2.2 g/100mL; 14 g/100mL 60954-0012-08 | PT. | 1 bottle | — | — | FDA listed | — |
| Eagle Brand Eagle Balm 4 g/100g; 15.5 g/100g 60954-0201-20 | PT. | 1 jar | — | — | FDA listed | — |
| Ramedica Herbal Wonder Balm 10.8 g/100g; 11 g/100g 66059-0005-01 | Ramedicare | 1 bottle | — | — | FDA listed | — |
| Ay Bendito - Pain Relief 4 g/100g; 6 g/100g 72524-0640-04 | AY | 113 g | — | — | FDA listed | — |
| PM Recovery Pain Relief 15 g/100g; 10 g/100g 79845-0770-30 | Charlotte's | 30 g | — | — | FDA listed | — |
| PlusCBD Pain Cream (Penetrating) 2oz 10 g/100g; 11 g/100g 82026-0611-58 | CV | 1 tube | — | — | FDA listed | — |
| MYCO Clinic Pain Relief 11 g/100g; 16 g/100g 24909-0013-17 | Aidance | 10 packets | — | — | FDA listed | — |
| Eagle Brand Medicated Oil Refresh 14 g/100mL; 2.2 g/100mL 43405-0013-24 | Borden | 1 bottle | — | — | FDA listed | — |
| Zepol Topical Analgesic 6.55 g/100g; 6.55 g/100g 55715-0001-01 | Laboratorios | 30 g | — | — | FDA listed | — |
| Camphotrex 4 g/100g; 10 g/100g 59088-0283-07 | PureTek | 85 g | — | — | FDA listed | — |
| Professional Therapy MuscleCare Pro Roll-on 4 g/100g; 10 g/100g 70039-0301-03 | ACTIVE | 85 g | — | — | FDA listed | — |
| Ay Bendito - Cbd 4 g/100g; 6 g/100g 72524-0009-04 | AY | 90.15 g | — | — | FDA listed | — |
| Ay Bendito - Cbd 6 g/100g; 4 g/100g 72524-0064-04 | AY | 113 g | — | — | FDA listed | — |
| Ay Bendito Hemp Roll-On 4 g/100g; 6 g/100g 72524-0091-03 | AY | 90.15 g | — | — | FDA listed | — |
| Ay Bendito - Thermoactive 4 g/100g; 6 g/100g 72524-0604-04 | AY | 90 g | — | — | FDA listed | — |
| HERSTAT GST Genital Sore Treatment 3 g/100g; .1 g/100g 90100-0222-14 | Herstat | 1 tube | — | — | FDA listed | — |
| Softlips Naturals Medicated 5 mg/g; 10 mg/g 10742-8481-01 | The | 2 tubes | — | — | FDA listed | — |
| CVS Anti-Itch .5 g/100g; .5 g/100g 69842-0626-75 | CVS | 212 g | — | — | FDA listed | — |
| Active Recovery Pain Relief Stick 10 g/100g; 15 g/100g 79845-0769-30 | Charlottes | 30 g | — | — | FDA listed | — |
| Dragon Pain Relieving Balm 10 g/100g; 11 g/100g 83552-0115-00 | AMERICANNA | 96.4 g | — | — | FDA listed | — |
| MYCO Clinic Pain Relief 3.1 g/100mL; 7 g/100mL 24909-0011-10 | Aidance | 100 ml | — | — | FDA listed | — |
| Camphotrol 4 g/100g; 10 g/100g 59088-0488-07 | PureTek | 85 g | — | — | FDA listed | — |
| Walgreen Anti Itch .5 g/100g; .5 g/100g 00363-4262-75 | Walgreens | 212 g | — | — | FDA listed | — |
| Softlips Naturals Medicated Matcha Honey 10 mg/g; 5 mg/g 10742-8480-01 | The | 2 tubes | — | — | FDA listed | — |
| ICY Hot Pro No Mess Two Pack 11 g/100g; 6 g/100g 41167-7181-05 | Chattem, | 2 tubes | — | — | FDA listed | — |
| Tylenol Precise Nighttime Pain Relieving 40 mg/g; 12.5 mg/g 69968-0905-04 | Kenvue | 1 tube | — | — | FDA listed | — |
| Ay Bendito Hemp 6 g/100g; 4 g/100g 72524-0092-04 | AY | 113 g | — | — | FDA listed | — |
| Paingel 10 g/100g; 6 g/100g 85110-0610-04 | NACOR | 113 g | — | — | FDA listed | — |
| Icy Hot Pro No-Mess 11 g/100g; 16 g/100g 41167-0079-06 | Chattem, | 85 g | — | — | FDA listed | — |
| Discount Drug Mart Anti-Itch .5 g/100g; .5 g/100g 53943-0262-75 | Discount | 212 g | — | — | FDA listed | — |
| Eagle Brand Medicated Roll On Refresh 12.18 g/100mL; 1.91 g/100mL 43405-0098-08 | Borden | 1 bottle | — | — | FDA listed | — |
| Eagle Brand Medicated Oil Refresh 1.91 g/100mL; 12.18 g/100mL 43405-0097-03 | Borden | 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
🏛️
2026
On the market since
Apr 2026
📍
2026
Currently FDA-listed
listed with the FDA
🔒
·
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 CVS Muscle Balm and Roll-On (this brand).
Top reported reactions
Age at onset
Reporter sex
Male · 63%
Female · 38%
Serious outcomes
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 |
|---|---|---|---|
| 51316-0241-01 You're viewing this | 1 KIT in 1 CARTON (51316-241-01) * 74 mL in 1 BOTTLE, WITH APPLICATOR (51316-244-25) * 18 g in 1 JAR (51316-243-63) | 2026-04-13 | Active |
🧭 About this NDC listing & data coverage
Over-the-counter (OTC) product
Kit / multi-component package
Kit / multi-component package
This NDC identifies a kit — a package containing more than one component. Structured data (pricing, ingredients, equivalents) is often reported per component rather than for the kit NDC itself, which can make this page look thinner than the components' own pages.
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 FDA registers it as 51316-241-01, 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: 51316-0241-01, written without dashes as 51316024101. 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 51316-0241-01, the first segment (51316) is the labeler code FDA assigned to CVS Pharmacy; the middle segment (0241) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (01) 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 CVS Pharmacy. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
CVS Pharmacy 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 ▾
Uses For the temporary relief of minor aches and pains of mucles and joints associated with simple backache, arthritis, strains, bruises, and sprains
⏱️ Dosage and Administration ▾
Directions Adults and children 12 years of age and older: Rub on affected area not more than 3 to 4 times daily. Children under 12 years of age: consult a doctor before use.
⚠️ Warnings ▾
Warnings For external use only When using this product avoid contact with eyes and mucous membranes do not apply to open wounds or damaged skin do not bandage or use a heating pad Stop use and ask a doctor if condition worsens severe skin irritation occurs pain persists for more than seven days or clears up and recurs a few days later 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 Posion Control Center right away.
🧪 Active Ingredient ▾
Active ingredients Camphor 11% Menthol 11%
🧪 Inactive Ingredients ▾
Inactive ingredients - Pain Relieving Balm Cinnamomum Cassia Leaf Oil, Eugenia Caryophyllus Bud Oil, Melaleuca Leucadendron Cajuputi Leaf Oil, Mentha Arvensis Leaf Oil, Paraffin, Petrolatum
Inactive ingredients - Pain Relieving Roll-On Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Cinnamomum Cassia Leaf Oil, Eugenia Caryophyllus Bud Oil, Melaleuca Leucadendron Cajuputi Leaf Oil, Mentha Arvensis Leaf Oil, SD Alcohol 40-B, Water
🎯 Purpose ▾
Purposes Topical analgesic Topical analgesic
No label section mentions that — try another word, or open the full label on DailyMed below.
Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA.
Prefer the government’s original formatting? View this label on DailyMed ↗
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.