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terrasil Bruise and Pain Relief Maximum Strength Camphor, Menthol 16 g/100g; 11 g/100g Ointment, 50 g — NDC 24909-0042-50 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

terrasil Bruise and Pain Relief Maximum Strength Camphor, Menthol 16 g/100g; 11 g/100g Ointment, 50 g — NDC 24909-042-50 (Billing 24909-0042-50)

by Aidance Scientific, Inc., DBA Aidance Skincare & Topical Solutions · 50 g in 1 TUBE

This is a package of 50 g of terrasil Bruise and Pain Relief Maximum Strength Camphor, Menthol 16 g/100g; 11 g/100g Ointment from Aidance Scientific, Inc., DBA Aidance Skincare & Topical Solutions, marketed since Oct 2024 and currently FDA-listed. It is this product's only package size.

NDC 24909-0042-50
🏷️ FDA NDC (as labeled) 24909-042-50 billing pads the product segment with a zero
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) 24909-042-50
Product NDC 24909-042
11-digit billing NDC 24909004250
RxCUI 1802734
UNII L7T10EIP3A, N20HL7Q941
Application # M017
SPL Set ID 240b231d-a8b2-c64c-e063-6394a90a7440
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2024-10-21
Route TOPICAL
Dosage form OINTMENT
Substance MENTHOL; CAMPHOR (NATURAL)
Quick answers
  • RxCUI (RxNorm): 1802734
Why two NDCs? The FDA registers this code as 24909-042-50 — 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 → 24909-0042-50. 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.

Clinical

🧪 What is this product?

Terrasil Bruise and Pain Relief Maximum Strength is a topical ointment containing camphor and menthol. This product is an over-the-counter monograph drug, meaning it is marketed under FDA's established rules for this category of ointment rather than as an individually reviewed application. Camphor and menthol are counterirritants commonly used in topical products intended to produce a warming or cooling sensation on the skin, and both have a long history in over-the-counter pain relief formulations.

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.
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
24909-0042-50 You're viewing this Main listing 50 g in 1 TUBE 2024-10-21 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
MYCO Clinic Pain Relief 11 g/100g; 16 g/100g 24909-0012-50 Aidance 50 g — — FDA listed —
MYCO Clinic Pain Relief 11 g/100g; 16 g/100g 24909-0013-17 Aidance 10 packets — — FDA listed —
terrasil Bruise and Pain Relief Maximum Strength 16 g/100g; 11 g/100gthis 24909-0042-50 Aidance 50 g — — FDA listed —
Active Recovery Pain Relief 16 g/100g; 11 g/100g 79845-0768-44 Charlotte's 44 g — — FDA listed —
Paingel Unguento 11 g/100g; 16 g/100g 85110-0116-04 NACOR 113 g — — 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

🏛️
2024
On the market since
Oct 2024
📍
2026
Currently FDA-listed
2 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 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 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 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 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 2ZA36H0S2V
    Beeswax is a natural wax produced by honeybees. In medicines, it works as a coating agent and thickener to control how fast the drug dissolves and improve the product's texture and appearance.

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

The official label also statesarnica extract, beeswax, colloidal oatmeal, ginger extract, honeysuckle oil, jojoba oil, MCT/coconut oil, mushroom extracts - USDA organic (cordyceps, lion's mane, reishi, shiitake), sorbic acid, sunflower oil, sweet orange oil, turmeric extract

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

LabelerAidance Scientific, Inc., DBA Aidance Skincare & Topical Solutions
FDA applicationM017 (OTC MONOGRAPH DRUG)
Labeler code24909
First marketedOct 2024
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.

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 📄 Do Not Use 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 🤰 If Pregnant or Breast-Feeding 📄 Keep Out of Reach of Children 📄 Other Information 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 14 words ▾

Uses Temporarily relieves minor aches and pain of muscles and joints associated with bruises.

⏱️ Dosage and Administration 44 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 93 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 11 words ▾

Active ingredients Camphor USP, 11%, Menthol USP, 16% Purpose Topical analgesic

🧪 Inactive Ingredients 34 words ▾

Inactive ingredients arnica extract, beeswax, colloidal oatmeal, ginger extract, honeysuckle oil, jojoba oil, MCT/coconut oil, mushroom extracts - USDA organic (cordyceps, lion's mane, reishi, shiitake), sorbic acid, sunflower oil, sweet orange oil, turmeric extract

🎯 Purpose 3 words ▾

Purpose Topical analgesic

📄 Do Not Use 8 words ▾

Do not use on wounds or damaged skin.

📄 When Using This Product 21 words ▾

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 30 words ▾

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 Breast-Feeding 11 words ▾

If pregnant or breastfeeding , ask a health professional before use.

📄 Keep Out of Reach of Children 6 words ▾

Keep out of reach of children.

📄 Other Information 12 words ▾

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

📄 Package Label / Principal Display Panel 11 words ▾

terrasil Bruise & Pain Relief Maximum Strength 50g Tube Product Label

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

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

Serious outcomes

Hospitalization121
Disabling22
Life-threatening12
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 44 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: 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.
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.
← 24909-0041-10 · Aidance 24909-0043-28 · 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.