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MYCO Clinic Pain Relief Menthol 4 g/100g Cream, 50 g — NDC 24909-0010-50 package photo

MYCO Clinic Pain Relief Menthol 4 g/100g Cream, 50 g

by Aidance Scientific, Inc., DBA Aidance Skincare & Topical Solutions · 50 g in 1 TUBE (24909-010-50)
NDC 24909-0010-50
🏷️ FDA NDC (as labeled) 24909-010-50 billing pads the product segment with a zero
This package
Contains50 g Pack sizes2 compare ↓
Also comes in: 200 g 24909-0010-20
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 →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

⚠️
Other active recalls for Menthol (different manufacturers) — 1 · tap to view
These affect other manufacturers’ products for the same ingredient — not necessarily the exact NDC on this page.
Class II · Mar 20, 2026 — This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing facility that may bear on product quality. (Xiamen Kang Zhongyuan Biotechnology Co., Ltd.) · FDA recall D-0458-2026
Each entry is an official FDA enforcement report — look up any recall number in the FDA recall database ↗

🆔 Identity & classification

FDA NDC (as labeled) 24909-010-50
Product NDC 24909-010
11-digit billing NDC 24909001050
RxCUI 1148430
UNII L7T10EIP3A
Application # M017
SPL Set ID 604a30c9-2306-47a1-bd31-94b63639dd90
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2023-02-24
Route TOPICAL
Dosage form CREAM
Substance MENTHOL
Why two NDCs? The FDA registers this code as 24909-010-50 — 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 → 24909-0010-50. 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

LabelerAidance Scientific, Inc., DBA Aidance Skincare & Topical Solutions
FDA applicationM017 (OTC MONOGRAPH DRUG)
Labeler code24909
First marketedFeb 2023
Product typeHuman Otc Drug
Portfolio19 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

📗 Our plain-language guide HelloPharmacist
  • Menthol is found in a lot of over-the-counter topical products — creams, gels, patches, sprays, and powders. Depending on the product, it's used to temporarily ease minor muscle an...
  • Start with clean, dry skin — free of lotions or creams — before applying the patch. Peel the backing off and press the sticky side firmly to the sore area. Most menthol patches sho...
  • Yes, a mild burning or tingling feeling right after applying a menthol product is common and usually settles down within a few days of regular use. What's not normal is severe burn...
  • Is that burning sensation after I apply it normal?
📖 Read our full Menthol guide →

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.

🧪 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 636VYW51FP
    Plant extract from Canadian columbine flower. Used as a natural coloring agent or flavoring component in some formulations to provide color or taste to the medicine.
  • UNII OZ0E5Y15PZ
    A plant extract from arnica flowers, used as a flavoring agent or fragrance component in medicines. It may also provide mild soothing properties to certain topical formulations.
  • UNII N20HL7Q941
    Camphor is a waxy, aromatic substance derived from camphor tree wood or made synthetically. In medicines, it typically serves as a preservative, flavoring agent, or mild skin irritant in topical products.
  • UNII 2DMT128M1S
    A waxy solid derived from plant or animal sources. It acts as an emulsifier to blend oil and water components, and also thickens the medicine to give it the right texture and consistency.
  • UNII Q9L0O73W7L
    Coconut oil is a natural fat extracted from coconut fruit. It's used in medicines as a lubricant, emollient, or carrier to help dissolve or deliver active ingredients smoothly through the formulation.
  • UNII 54C8E6W6JY
    A dried fungus ingredient used as a filler and nutritional additive in some formulations. It adds bulk and may contribute vitamins and minerals to the product.
  • UNII C5529G5JPQ
    Ginger is a plant-derived ingredient used as a flavoring agent to add taste and aroma to medicines. It may also provide mild soothing properties to support product palatability.
  • UNII BU6Y4J4C2E
    A fungal ingredient derived from the fruiting body of the lion's mane mushroom. It is used as a filler and nutritional component in supplements to add bulk and provide bioactive compounds to the formulation.
  • UNII 724GKU717M
    Jojoba oil is a natural liquid wax extracted from jojoba plant seeds. It's used in medicines as an emollient and lubricant to soften and smooth the product, and sometimes as a carrier or penetration enhancer.
  • UNII 8PI54V663Y
    Oatmeal is ground oat grain used as a natural filler and texture agent in medicines. It absorbs moisture, adds bulk to the formulation, and may help create a soothing base in topical products.
  • UNII 8Q1GYP08KU
    A fungus that grows on caterpillars in high-altitude regions, used in traditional medicine formulations. It may serve as an active botanical ingredient rather than a typical inactive excipient.
  • UNII AKN3KSD11B
    Orange oil obtained by cold pressing orange peel. It serves as a flavoring agent and fragrance in medicines to improve taste and aroma.
  • UNII TKD8LH0X2Z
    Reishi is a mushroom extract used in supplements and some medicines. It may function as a filler or active botanical ingredient, though its primary role in formulations is often to add volume or provide traditional plant-based content.
  • UNII K49155WL9Y
    Shea butter is a fat extracted from shea tree nuts. It's used in medicines as an emollient and lubricant to soften the product, improve texture, and help ingredients blend smoothly together.
  • UNII 1A64QN2D2F
    A fungal ingredient derived from shiitake mushrooms, used as a natural flavoring agent and potential nutritional component in formulations. It may contribute taste, aroma, and texture to the finished product.
  • UNII X045WJ989B
    Sorbic acid is a preservative derived from berries that prevents mold, yeast, and bacterial growth in medicines. It keeps the product stable and safe during storage.
  • UNII 3W1JG795YI
    Sunflower oil is a natural vegetable oil derived from sunflower seeds. It serves as a solvent, lubricant, and carrier in medicines, helping dissolve active ingredients and improve how the medication flows and absorbs in the body.
  • UNII 856YO1Z64F
    Turmeric is a natural spice derived from the turmeric plant root. It serves as a colorant in medicines, giving products a yellow or golden appearance, and may also provide mild flavoring.
  • UNII 059QF0KO0R
    Water is a liquid solvent that dissolves and mixes ingredients together in liquid medicines, syrups, and injections. It helps distribute the active drug evenly throughout the product.

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

The official label also statesArnica Extract, Colloidal Oatmeal, Ginger Extract, Honeysuckle Oil, Jojoba Oil, MCT/Coconut Oil, Mushroom Extracts - USDA Organic (Cordyceps, Lion's Mane, Reishi, Shiitake), Purified Water, Shea Butter, Sorbic Acid, Sunflower Oil, Sweet Orange Oil, Turmeric Extract, Camphor, Emulsifying Wax

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.

💲 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: 200 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.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
MYCO Clinic Pain Relief 4 g/100gthis 24909-0010-50 Aidance 50 g — — FDA listed —
Lightning Pain Relief 40 mg/g 63742-0013-00 Clinical 65 g — — FDA listed —
Dr. Carrasco Pain Relief 40 mg/mL 69921-0024-01 Carrasco 89 ml — — FDA listed —
Lightning Pain Relief 40 mg/g 72654-0013-00 Ebanel 65 g — — FDA listed —
Ease Your Pain 4 g/100g 72683-0002-01 Proximity 1 tube — — FDA listed —
Nerve Reverse Pain Relief 40 mg/mL 73067-0870-04 Pogue 118 ml — — FDA listed —
Comforte Menstrual Cramp Relief Cream 40 mg/g 73603-0000-00 PMS4PMS 1 tube — — FDA listed —
Toast Screamin Menthol 4 g/100g 78983-0103-05 IDEAZ, 148 g — — FDA listed —
Neuropathy Cream 4 g/100g 83570-0001-01 Owell 1 g — — FDA listed —
TIDL PAIN RELIEF CRYOTHERAPY MENTHOL Cream 4 g/100mL 84214-0009-01 Shenzhen 90 ml — — FDA listed —
AVCOO Pain Relief Roll-on 4 g/100mL 84992-0001-01 ADP 74 ml — — FDA listed —
Pain Relieving 4 g/100g 61010-4403-01 Safetec 113.4 g — — FDA listed —
Dragon with Arnical Pain Relief 4 g/100g 50066-0621-56 Genomma 1 tube — — 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
Feb 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.

🔬 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 MYCO Clinic Pain Relief (this brand).

Top reported reactions

Dyspnoea86
Fatigue84
Pain81
Pruritus78
Dizziness67
Headache67
Cough65

Reporter sex

997 reports

Serious outcomes

Death126
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 110 67
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 NDCDescription Marketing startStatus
24909-0010-20 200 g in 1 TUBE (24909-010-20) 2023-02-24 Active
24909-0010-50 You're viewing this 50 g in 1 TUBE (24909-010-50) 2023-02-24 Active

You're viewing the smallest of 2 pack sizes for this product.

Pack size FAQ

What quantity is in NDC 24909-0010-50?
NDC 24909-0010-50 contains 50 g — 50 g in 1 tube.
What is the difference between NDC 24909-0010-50 and NDC 24909-0010-20?
Both are MYCO Clinic Pain Relief Menthol 4 g/100g Cream — the drug itself is identical. NDC 24909-0010-50 is the 50 g package, while NDC 24909-0010-20 is the 200 g package.
What NDC number is used to bill for this package of MYCO Clinic Pain Relief Menthol 4 g/100g Cream?
Bill NDC 24909-0010-50 — the 11-digit billing format is 24909001050. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

🧭 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 FDA registers it as 24909-010-50, 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: 24909-0010-50, written without dashes as 24909001050. 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 24909-0010-50, the first segment (24909) is the labeler code FDA assigned to Aidance Scientific, Inc., DBA Aidance Skincare & Topical Solutions; the middle segment (0010) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (50) 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 Aidance Scientific, Inc., DBA Aidance Skincare & Topical Solutions. 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 200 g (24909-0010-20). 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?
Aidance Scientific, Inc., DBA Aidance Skincare & Topical Solutions 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
🎯 Indications and Usage 19 words ▾

Uses temporarily relieves minor aches and pain of muscles and joints associated with: simple backache, arthritis, strains, bruises, sprains

⏱️ Dosage and Administration 43 words ▾

Directions adults and children 12 years of age and older: Apply to affected area not more than 3 to 4 times daily. Wash hands with soap and water after use (unless applying to hands) children under 12 years of age: ask a doctor

⚠️ Warnings 95 words ▾

Warnings For external use only Do not use on wounds or damaged skin When using this product avoid contact with eyes or mucous membranes - do not bandage tightly or use with a heating pad Stop use and ask a doctor if condition worsens, symptoms persist for more than 7 days, symptoms clear up and occur again within a few days, excessive skin irritation develops If pregnant or breastfeeding , ask a health professional before use. Keep out of reach of children . If swallowed, get medical help or contact a Poison Control Center immediately.

🧪 Active Ingredient 7 words ▾

Active Ingredients Purpose Menthol USP, 4%..........Topical analgesic

🧪 Inactive Ingredients 40 words ▾

Inactive ingredients Arnica Extract, Colloidal Oatmeal, Ginger Extract, Honeysuckle Oil, Jojoba Oil, MCT/Coconut Oil, Mushroom Extracts - USDA Organic (Cordyceps, Lion's Mane, Reishi, Shiitake), Purified Water, Shea Butter, Sorbic Acid, Sunflower Oil, Sweet Orange Oil, Turmeric Extract, Camphor, Emulsifying Wax

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 24887-0001-01 · Superior 24909-0011-10 · Aidance →
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.