Home › NDC Lookup › Ingredients › Menthol Camphor › 51316-0240-02
CVS Muscle Balm Menthol, Camphor 110 mg/g; 110 mg/g Ointment — NDC 51316-0240-02 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

CVS Muscle Balm Menthol, Camphor 110 mg/g; 110 mg/g Ointment — NDC 51316-240-02 (Billing 51316-0240-02)

by CVS Health · 2 JAR in 1 CARTON / 18 g in 1 JAR

This is a package of CVS Muscle Balm Menthol, Camphor 110 mg/g; 110 mg/g Ointment from CVS Health, marketed since Mar 2026 and currently FDA-listed.

NDC 51316-0240-02
🏷️ FDA NDC (as labeled) 51316-240-02 billing pads the product segment with a zero
This package
Contains18 g in 1 jar Pack sizes2 compare ↓
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 →

NDC database record

One package, one record: these facts belong to NDC 51316-240-02 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
51316 labeler · 240 product · 02 package
Package marketed since
Mar 16, 2026
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC)
0050428566138
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 51316-240-02
Product NDC 51316-240
11-digit billing NDC 51316024002
RxCUI 1089847
UNII L7T10EIP3A, 5TJD82A1ET
UPC 0050428566138
Application # M017
SPL Set ID 42796fc4-03be-3b02-e063-6394a90af2ab
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-03-16
Route TOPICAL
Dosage form OINTMENT
Substance MENTHOL, UNSPECIFIED FORM; CAMPHOR (SYNTHETIC)
Quick answers
  • RxCUI (RxNorm): 1089847
Why two NDCs? The FDA registers this code as 51316-240-02 — 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 → 51316-0240-02. 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?

CVS Muscle Balm Menthol is a topical ointment containing menthol and camphor. These ingredients are commonly used in over-the-counter rubs and balms and are typically applied to the skin to produce a warming or cooling sensation. This product is marketed as an OTC monograph drug, meaning it follows established FDA guidelines for this category of topical pain-relief products rather than being approved through an individual application process.

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: 18 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
51316-0240-01 51316-240-01 Main listing 1 JAR in 1 CARTON / 18 g in 1 JAR 2026-03-16 — Active
51316-0240-02 You're viewing this 2 JAR in 1 CARTON / 18 g in 1 JAR 2026-03-16 — Active

Pack size FAQ

What quantity is in this package?
This package is listed by the FDA — 2 jar in 1 carton / 18 g in 1 jar.
What NDC number is used to bill for this package of CVS Muscle Balm Menthol, Camphor 110 mg/g; 110 mg/g Ointment?
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
CVS Muscle Balm 110 mg/g; 110 mg/gthis 51316-0240-02 CVS 2 jars — — FDA listed —
CVS Muscle Balm and Roll-On 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 —
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
Mar 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.

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 J3TO6BUQ37
    Cajuput oil is a fragrant essential oil extracted from the cajuput tree. It's used in medicines as a flavoring agent and to add aroma, and may help mask unpleasant tastes.
  • UNII A4WO0626T5
    A natural aromatic oil extracted from cinnamon bark, used as a flavoring agent to improve taste and add spice notes to medicines.
  • UNII 578389D6D0
    Clove oil is an essential oil derived from clove plant buds. It's used in medicines as a flavoring agent and for its mild preservative properties to help maintain product stability.
  • UNII I9O0E3H2ZE
    Paraffin is a waxy, petroleum-derived substance used as a coating, lubricant, and hardening agent in tablets and capsules. It helps protect the medicine from moisture and gives pills a smooth finish.
  • UNII 4CA0UO1N3Z
    A plant-derived oil from peppermint with volatile compounds removed, leaving behind the flavor and aroma components. Used in medicines as a flavoring agent to improve taste and mask bitter drug flavors.
  • UNII 4T6H12BN9U
    Petrolatum is a purified mineral oil-based jelly derived from petroleum. In medicines, it acts as an emollient, lubricant, and moisture barrier to soften skin, reduce friction, and help prevent water loss from formulations.

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

The official label also statesCinnamomum Cassia Leaf Oil, Eugenia Caryophyllus Bud Oil, Melaleuca Leucadendron Cajuputi Leaf Oil, Mentha Arvensis Leaf Oil, Paraffin, Petrolatum

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

LabelerCVS Health
FDA applicationM017 (OTC MONOGRAPH DRUG)
Labeler code51316
First marketedMar 2026
Product typeHuman Otc Drug
Portfolio50 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 23 words ▾

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

⏱️ Dosage and Administration 33 words ▾

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 118 words ▾

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 Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately If pregnant or breast-feeding, ask a healthcare professional before use.

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

🧪 Active Ingredient 6 words ▾

Active ingredients Camphor 11% Menthol 11%

🧪 Inactive Ingredients 21 words ▾

Inactive ingredients Cinnamomum Cassia Leaf Oil, Eugenia Caryophyllus Bud Oil, Melaleuca Leucadendron Cajuputi Leaf Oil, Mentha Arvensis Leaf Oil, Paraffin, Petrolatum

🎯 Purpose 5 words ▾

Purposes Topical analgesic Topical analgesic

📄 Stop Use and Ask a Doctor If 29 words ▾

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 10 words ▾

If pregnant or breast-feeding, ask a healthcare 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

📄 Other Information 17 words ▾

Other information This product may cause allergic reactions in some individuals. Test on small area before use.

📄 Package Label / Principal Display Panel 117 words ▾

Principal Display Panel - 2 x 18 g Carton Label CVS TM Ultra Strength Muscle Balm Camphor 11%, Menthol 11% Pain Relieving Ointment Compare to Tiger Balm ® Ultra Strength active ingredients † Temporary Muscle Pain Relief From: Backaches Arthritis Joint pain Bruises Strains, Sprains NET WT 2 X

0.63 OZ (18 g) | TOTAL NET WT

1.26 OZ (37 g) Carton

Principal Display Panel - 18 g Carton Label CVS Health TM Compare to the active ingredient in Tiger Balm ® * Intense Strength Muscle Balm Pain Relieving Ointment Relieves pain where it hurts Temporary muscle pain relief from: Backaches Arthritis Joint pain Bruises Strains Sprains NET WT

0.63 OZ (18 g) 18 g Carton 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
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 CVS Health. 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 1 jar (51316-0240-01). 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?
CVS Health 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.
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.