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Eagle Brand Medicated Oil Refresh camphor, menthol 14 g/100mL; 2.2 g/100mL Oil — NDC 60954-0013-36 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Eagle Brand Medicated Oil Refresh camphor, menthol 14 g/100mL; 2.2 g/100mL Oil — NDC 60954-013-36 (Billing 60954-0013-36)

by PT. EAGLE INDO PHARMA · 1 BOTTLE, GLASS in 1 BOX / 36 mL in 1 BOTTLE, GLASS

This is a package of Eagle Brand Medicated Oil Refresh camphor, menthol 14 g/100mL; 2.2 g/100mL Oil from PT. EAGLE INDO PHARMA, marketed since Nov 2023 and currently FDA-listed.

NDC 60954-0013-36
🏷️ FDA NDC (as labeled) 60954-013-36 billing pads the product segment with a zero
This package
Contains36 mL in 1 bottle, glass Pack sizes2 compare ↓
Product page 60954-0013-24 Also comes in: 24 mL 60954-013-24
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Aug 27, 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) 60954-013-36
Product NDC 60954-013
11-digit billing NDC 60954001336
RxCUI 2672336
UNII L7T10EIP3A, 5TJD82A1ET
UPC 8888951888616
Application # M017
SPL Set ID 09260c31-56a3-07aa-e063-6394a90a95fd
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2023-11-02
Route TOPICAL
Dosage form OIL
Substance MENTHOL; CAMPHOR (SYNTHETIC)
Quick answers
  • RxCUI (RxNorm): 2672336
Why two NDCs? The FDA registers this code as 60954-013-36 — 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 → 60954-0013-36. 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?

Eagle Brand Medicated Oil Refresh is a topical oil containing camphor and menthol. This product is an over-the-counter monograph drug, meaning it follows FDA's established rules for this class of medicine rather than undergoing individual approval. Camphor and menthol are commonly used in topical preparations for their cooling and warming sensations on the skin. These ingredients are typically found in products applied to the skin surface to provide localized comfort.

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.
Try another pack size: 24 mL
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
60954-0013-24 60954-013-24 Main listing 1 BOTTLE, GLASS in 1 BOX / 24 mL in 1 BOTTLE, GLASS 2023-11-02 — Active
60954-0013-36 You're viewing this 1 BOTTLE, GLASS in 1 BOX / 36 mL in 1 BOTTLE, GLASS 2023-11-02 — Active

Pack size FAQ

What quantity is in this package?
This package is listed by the FDA — 1 bottle, glass in 1 box / 36 ml in 1 bottle, glass.
What NDC number is used to bill for this package of Eagle Brand Medicated Oil Refresh camphor, menthol 14 g/100mL; 2.2 g/100mL Oil?
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
Eagle Brand Medicated Roll On Refresh 2.2 g/100mL; 14 g/100mL 43405-0012-08 Borden 1 bottle — — FDA listed —
Eagle Brand Medicated Oil Refresh 14 g/100mL; 2.2 g/100mL 43405-0013-24 Borden 1 bottle — — 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 Medicated Oil Refresh 14 g/100mL; 2.2 g/100mLthis 60954-0013-36 PT. 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

🏛️
2023
On the market since
Nov 2023
📍
2026
Currently FDA-listed
3 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 01YAE03M7J
    Beta carotene is a naturally occurring orange pigment found in plants. In medicines, it serves as a colorant to make tablets or capsules appear orange or yellow.
  • 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 ND733RX3JN
    A synthetic red colorant used to give medicines their color. It helps identify the medication and makes it visually distinguishable from other drugs.
  • UNII N6K5787QVP
    Light mineral oil is a clear, odorless liquid derived from petroleum. In medicines, it acts as a lubricant and emollient to help the product spread smoothly and improve texture.
  • UNII AV092KU4JH
    A natural oil extracted from peppermint plants. It's used as a flavoring agent to mask bitter tastes and add a refreshing mint flavor to medicines, making them easier to take.

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

The official label also statesbeta carotene, clove oil, D&C Red No.17, fragrance, light mineral oil, peppermint oil

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

LabelerPT. EAGLE INDO PHARMA
FDA applicationM017 (OTC MONOGRAPH DRUG)
Labeler code60954
First marketedNov 2023
Product typeHuman Otc Drug
Portfolio13 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 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 🤰 If Pregnant or Breast-Feeding 📄 Keep Out of Reach of Children 📄 Other Information 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 33 words ▾

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

⏱️ Dosage and Administration 36 words ▾

Directions • Adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily. • Children under 2 years of age: do not use, consult a doctor.

⚠️ Warnings 107 words ▾

Warnings For external use only When using this product • Avoid getting into the eyes or on mucous membranes. • Do not apply to wounds or damaged skin. • Do not bandage tightly. • Do not use otherwise than as directed. Stop use and ask a doctor if Condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a doctor. Keep out of reach of children If swallowed, get medical help or contact a Poison Control Centre right away.

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

🧪 Active Ingredient 6 words ▾

Active ingredients Camphor 2.2% Menthol 14%

🧪 Inactive Ingredients 15 words ▾

Inactive ingredients beta carotene, clove oil, D&C Red No.17, fragrance, light mineral oil, peppermint oil

🎯 Purpose 3 words ▾

Purpose External Analgesic

📄 When Using This Product 36 words ▾

When using this product • Avoid getting into the eyes or on mucous membranes. • Do not apply to wounds or damaged skin. • Do not bandage tightly. • Do not use otherwise than as directed.

📄 Stop Use and Ask a Doctor If 37 words ▾

Stop use and ask a doctor if Condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a doctor.

🤰 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 Centre right away.

📄 Other Information 10 words ▾

Other information Store below 86 o F (30 o C).

📄 Questions or Comments 16 words ▾

Questions? If there are any questions or to report serious side effects, call 1-800-777-6717 or 1-800-645-0769.

📄 Package Label / Principal Display Panel 14 words ▾

Package Label 24ml NDC: 60954-013-24 36ml NDC: 60954-013-36 24ml Unit Box 36ml Unit Box

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 PT. EAGLE INDO PHARMA. 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 bottle (60954-0013-24). 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?
PT. EAGLE INDO PHARMA 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.
← 60954-0012-08 · PT. 60954-0014-24 · PT. →
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.