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Ramedica Herbal Wonder Balm Camphor, Menthol 10.8 g/100g; 11 g/100g Ointment — NDC 66059-0005-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Ramedica Herbal Wonder Balm Camphor, Menthol 10.8 g/100g; 11 g/100g Ointment — NDC 66059-0005-1 (Billing 66059-0005-01)

by Ramedicare Sdn. Bhd. · 12 CARTON in 1 CASE / 12 BOX in 1 CARTON / 1 BOTTLE, GLASS in 1 BOX / 23 g in 1 BOTTLE, GLASS

This is a package of Ramedica Herbal Wonder Balm Camphor, Menthol 10.8 g/100g; 11 g/100g Ointment from Ramedicare Sdn. Bhd., marketed since Jul 2025 and currently FDA-listed, this package's marketing is listed to end Aug 2028. It is the main listing for this product, which comes in 2 package sizes.

NDC 66059-0005-01
🏷️ FDA NDC (as labeled) 66059-0005-1 billing pads the package segment with a zero
This package
Contains23 g in 1 bottle, glass Pack sizes2 compare ↓
Main listing for product 66059-0005 · Also comes in: 300 g 66059-0005-2
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 8, 2026 · this listing last changed Sep 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 66059-0005-1 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
66059 labeler · 0005 product · 1 package
Package marketed since
Jul 1, 2025
Package marketing ended
Aug 31, 2028
Sample package
No — commercial package
Barcode (UPC-A, from the NDC)
3 6605900051 5
FDA record last changed
Sep 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 66059-0005-1
Product NDC 66059-0005
11-digit billing NDC 66059000501
RxCUI 2717654
UNII N20HL7Q941, L7T10EIP3A
Application # M017
SPL Set ID cfb2ea0e-a1f6-4fdf-b866-346bbe78788f
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2025-07-01
Marketing end 2028-08-31
Route TOPICAL
Dosage form OINTMENT
Substance CAMPHOR (NATURAL); MENTHOL
Quick answers
  • RxCUI (RxNorm): 2717654
Why two NDCs? The FDA registers this code as 66059-0005-1 — a 5-4-1 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 package segment → 66059-0005-01. 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?

Ramedica Herbal Wonder Balm is an over-the-counter topical ointment containing camphor and menthol. This product is marketed as an OTC monograph drug, meaning it follows FDA's established category rules rather than undergoing individual review. Camphor and menthol are commonly used in topical preparations for their warming and cooling sensations, and are typically found in balms intended for localized application to skin.

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.
Try another pack size: 300 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
66059-0005-01 You're viewing this Main listing 12 CARTON in 1 CASE / 12 BOX in 1 CARTON / 1 BOTTLE, GLASS in 1 BOX / 23 g in 1 BOTTLE, GLASS 2025-07-01 Aug 31, 2028 Active
66059-0005-02 66059-0005-2 300 g in 1 JAR 2025-07-01 Aug 31, 2028 Active

Pack size FAQ

What quantity is in this package?
This package is listed by the FDA — 12 carton in 1 case / 12 box in 1 carton / 1 bottle, glass in 1 box / 23 g in 1 bottle, glass.
What NDC number is used to bill for this package of Ramedica Herbal Wonder Balm Camphor, Menthol 10.8 g/100g; 11 g/100g 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
Ramedica Herbal Wonder Balm 10.8 g/100g; 11 g/100gthis 66059-0005-01 Ramedicare 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

🏛️
2025
On the market since
Jul 2025
📍
2026
Currently FDA-listed
1 year 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 M89NIB437X
    Borneol is a waxy, plant-derived alcohol obtained from camphor trees or made synthetically. It's used in medicines as a flavoring agent and penetration enhancer to improve how active ingredients are absorbed.
  • 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 S92U8SQ71V
    A natural oil extracted from cinnamon leaves used as a flavoring agent and fragrance in medicines. It provides taste and aroma to make the product more pleasant to take.
  • UNII QYO8Q067D0
    Citronella oil is a natural plant-derived oil used as a fragrance and flavoring agent in medicines. It provides taste and aroma to make medications more palatable for patients.
  • 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 2R04ONI662
    Eucalyptus oil is a fragrant liquid extracted from eucalyptus tree leaves. It's used in medicines as a flavor, scent, or soothing agent in topical products and cough preparations.
  • UNII Z1CLM48948
    Nutmeg oil is a natural aromatic extract from nutmeg seeds. It's used in medicines as a flavoring agent to improve taste and sometimes as a fragrance to mask bitter or unpleasant odors.
  • 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 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.
  • UNII B6E5W8RQJ4
    White petrolatum is a purified mineral oil product used as a lubricant and skin protectant in medications. It helps pills slide through manufacturing equipment and can soften or protect the skin when applied topically.

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

The official label also statesBorneol, Cassia Oil, Cinnamon Leaf Oil, Citronella Oil, Clove Oil, Eucalyptus Oil, Nutmeg Oil, Paraffin Wax, Peppermint Oil, Soft White Paraffin

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

LabelerRamedicare Sdn. Bhd.
FDA applicationM017 (OTC MONOGRAPH DRUG)
Labeler code66059
First marketedJul 2025
Product typeHuman Otc Drug
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 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 25 words ▾

Uses For the temporary relief of minor aches & pains of muscles and joints associated with: arthritis & rheumatism backaches strains bruises sprains leg cramps

⏱️ Dosage and Administration 34 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 physician.

⚠️ Warnings 102 words ▾

Warnings For external use only. When using this product : Avoid contact with the eyes Do not apply to wounds or damaged skin Do not bandage tightly Do not use with heating pads or heating devices Stop use and consult 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 physician. If pregnant or breast-feeding , ask a health care professional before use Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control immediately

🧪 Active Ingredient 9 words ▾

Active Ingredients Camphor 10.8%................................Topical Analgesic Menthol Crystal 11%.........................Topical Analgesic

🧪 Inactive Ingredients 23 words ▾

Inactive Ingredients Borneol, Cassia Oil, Cinnamon Leaf Oil, Citronella Oil, Clove Oil, Eucalyptus Oil, Nutmeg Oil, Paraffin Wax, Peppermint Oil, Soft White Paraffin

📄 Package Label / Principal Display Panel 8 words ▾

Product label image description image description image description

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 — the ingredient across all brands.

Top reported reactions

Application Site Burn63
Pain53
Application Site Pain45
Burning Sensation34
Blister32
Fatigue29
Skin Burning Sensation29

Age at onset

Child5
Adolescent2
Adult102
Elderly37

Reporter sex

930 reports
Male · 32%
Female · 67%
Unknown · 1%

Serious outcomes

Hospitalization121
Life-threatening12
Reports over time (by year) — tap or hover for the count & year
2020 2022 2024 2026 221 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 it is currently marketed — but Ramedicare Sdn. Bhd. has reported a marketing end date of 2028-08-31, after which this package is expected to stop being marketed. 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 300 g (66059-0005-02). 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?
Ramedicare Sdn. Bhd. 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.
← 66051-0236-80 · Haws 66064-1001-01 · Harman →
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.