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Richtofit Rapid Active Arthritis Menthol and Camphor 5 g/100g; 4 g/100g Gel — NDC 87384-0058-10 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Richtofit Rapid Active Arthritis Menthol and Camphor 5 g/100g; 4 g/100g Gel — NDC 87384-058-10 (Billing 87384-0058-10)

by RICHTOFIT LIMITED LIABILITY COMPANY · 1 TUBE in 1 CARTON / 85 g in 1 TUBE

This is a package of Richtofit Rapid Active Arthritis Menthol and Camphor 5 g/100g; 4 g/100g Gel from RICHTOFIT LIMITED LIABILITY COMPANY, marketed since Mar 2026 and currently FDA-listed. It is this product's only package size.

NDC 87384-0058-10
🏷️ FDA NDC (as labeled) 87384-058-10 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) 87384-058-10
Product NDC 87384-058
11-digit billing NDC 87384005810
RxCUI 2739008
UNII L7T10EIP3A, 5TJD82A1ET
UPC 0860015386786
Application # M017
SPL Set ID 4b1cdab1-3e50-4ec3-e063-6394a90af75e
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-03-02
Route TOPICAL
Dosage form GEL
Substance MENTHOL; CAMPHOR (SYNTHETIC)
Quick answers
  • RxCUI (RxNorm): 2739008
Why two NDCs? The FDA registers this code as 87384-058-10 — 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 → 87384-0058-10. 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?

Richtofit Rapid Active Arthritis is a topical gel containing menthol and camphor that is applied directly to the skin. These ingredients are commonly included in over-the-counter products typically used to provide a warming or cooling sensation and may help with localized discomfort. This product is an OTC monograph drug, meaning it is marketed under established FDA guidelines for this category rather than through an individual product application.

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
87384-0058-10 You're viewing this Main listing 1 TUBE in 1 CARTON / 85 g in 1 TUBE 2026-03-02 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Richtofit Rapid Active Arthritis 5 g/100g; 4 g/100gthis 87384-0058-10 RICHTOFIT 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

🏛️
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.

What it looks like

Color white
One label can cover several strengths, so colors may be combined — always confirm a loose pill against the dispensed prescription label or a pharmacist.
Where does this data come from?
Physical description (imprint, shape, color, scoring, coating) from this product’s FDA Structured Product Labeling (SPL), mirrored from DailyMed / openFDA.

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 8Z5ZAL5H3V
    A synthetic polymer made from acrylate compounds. It acts as a thickener and stabilizer in topical formulations, helping create the right texture and prevent separation of ingredients.
  • UNII UB27587839
    A plant-derived oil from Roman chamomile flowers. It's used in medicines as a flavoring agent and fragrance to improve taste and smell.
  • 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 147D247K3P
    Ethylhexylglycerin is a synthetic preservative used to prevent bacteria and mold from growing in medicines and personal care products. It helps keep the product safe and stable throughout its shelf life.
  • UNII 5EM498GW35
    A mixture of aromatic compounds used to add pleasant smell to the medicine. Fragrance helps mask unpleasant tastes or odors, making the medication easier to take.
  • UNII PDC6A3C0OX
    Glycerin is a clear, thick liquid derived from plant oils or fats. It acts as a humectant to retain moisture, a sweetener, and a solvent in medications.
  • UNII 912A6Q1N4A
    Humulus lupulus, commonly known as hops, is a plant material used as a flavoring and aromatic agent in medicines. It may also provide mild preservative properties to help maintain product stability.
  • UNII 85HKB87105
    A plant extract from walnut tree leaves used as a natural colorant and antioxidant in medicines. It helps maintain product stability and may contribute to the pill or tablet's brown or tan color.
  • UNII 51217XIL5L
    A plant material derived from lavender flowers, used as a natural flavor and fragrance agent in medicines to improve taste and aroma.
  • UNII SA8AR2W4ER
    A natural oil extracted from chamomile flower tops, used as a flavoring and fragrance agent to improve taste and aroma in medicines.
  • UNII 3VNC7T6Z02
    A plant extract from chamomile flowers used as a flavoring and fragrance agent in medicines. It adds taste and aroma to improve how the medicine smells and tastes.
  • UNII HIE492ZZ3T
    Phenoxyethanol is a synthetic preservative and antimicrobial agent used to prevent bacterial and fungal growth in medicines and cosmetic products, extending shelf life and maintaining product safety.
  • UNII 7T1F30V5YH
    A synthetic emulsifier derived from sorbitol and oleic acid. It helps mix oil and water-based ingredients together and keeps them from separating in liquid formulations.
  • UNII I5G2JR395W
    A plant-derived ingredient from silverweed, used as a natural filler and binding agent to give the medication its physical form and help hold it together.
  • UNII R7QMG0BT2W
    A plant-derived substance from oak wood used as a natural colorant and flavoring agent in medicines. It may help provide color or taste to the final product.
  • UNII 065C5D077J
    Sage is a natural plant extract used in medicines as a flavoring agent and preservative. It may help mask bitter tastes and extend shelf life in certain formulations.
  • UNII 205MXS71H7
    A plant extract from white willow bark. It's used as a natural flavoring agent and may help preserve the medicine by providing mild antioxidant properties in the formulation.
  • UNII 55X04QC32I
    A strong alkaline chemical used to adjust and maintain the pH balance of liquid medicines. It helps keep the medicine stable and ensures it stays effective during storage.
  • UNII R0ZB2556P8
    Tocopherol is a form of vitamin E derived from plant oils. It acts as an antioxidant in medicines to prevent oils and fats from breaking down and spoiling during storage.
  • 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.

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

The official label also statesWater, Cetearyl Alcohol, Anthemis Nobilis Flower Oil, Chamomilla Recutita Flower Extract, Chamomilla Recutita Flower Oil, Humulus Lupulus Extract, Juglans Regia Leaf Extract, Lavandula Angustifolia Flower/Leaf/Stem Extract, Potentilla Anserina Extract, Quercus Robur Bark Extract, Salix Alba Bark Extract, Salvia Officinalis Leaf Extract, Glycerin, Cocos Nucifera Oil, Polysorbate 20, Phenoxyethanol, Fragrance, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Tocopherol, Sodium Hydroxide, Ethylhexylglycerin.

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

LabelerRICHTOFIT LIMITED LIABILITY COMPANY
FDA applicationM017 (OTC MONOGRAPH DRUG)
Labeler code87384
First marketedMar 2026
Product typeHuman Otc Drug
Portfolio2 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 📄 Questions or Comments 📖 Instructions for Use 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 21 words ▾

use Temporary relief of minor aches and pains of muscles and joints associated with arthritis, simple backache, strains, sprains, and bruises.

⏱️ Dosage and Administration 29 words ▾

Directions Adults and children 2 years of age and older: apply to affected area not more than 4 times daily. Children under 2 years of age: ask a doctor.

⚠️ Warnings 120 words ▾

Warnings For external use only When using this product Use only as directed. Avoid contact with eyes or mucous membranes. Do not use on wounds, damaged, or irritated skin.

Do not bandage or use with a heating pad. Do not use if you are allergic to any of the ingredients. Do not use with other ointments, creams, or sprays.

Stop use and ask a doctor if condition worsens, symptoms persist for more than 7 days, or clear up and occur again within a few days, or irritation or redness develops. If pregnant or breast-feeding ask a health professional before use. Keep out of reach of children If accidentally ingested, get medical help or contact a Poison Control Center right away.

🧪 Active Ingredient 12 words ▾

Active Ingredients Menthol 5% – External Analgesic Camphor 4% – External Analgesic

🧪 Inactive Ingredients 59 words ▾

Inactive Ingredients Water, Cetearyl Alcohol, Anthemis Nobilis Flower Oil, Chamomilla Recutita Flower Extract, Chamomilla Recutita Flower Oil, Humulus Lupulus Extract, Juglans Regia Leaf Extract, Lavandula Angustifolia Flower/Leaf/Stem Extract, Potentilla Anserina Extract, Quercus Robur Bark Extract, Salix Alba Bark Extract, Salvia Officinalis Leaf Extract, Glycerin, Cocos Nucifera Oil, Polysorbate 20, Phenoxyethanol, Fragrance, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Tocopherol, Sodium Hydroxide, Ethylhexylglycerin.

🎯 Purpose 3 words ▾

Purpose External Analgesic

📄 Do Not Use 39 words ▾

Do not use on wounds, damaged, or irritated skin. Do not bandage or use with a heating pad. Do not use if you are allergic to any of the ingredients. Do not use with other ointments, creams, or sprays.

📄 When Using This Product 15 words ▾

When using this product Use only as directed. Avoid contact with eyes or mucous membranes.

📄 Stop Use and Ask a Doctor If 31 words ▾

Stop use and ask a doctor if condition worsens, symptoms persist for more than 7 days, or clear up and occur again within a few days, or irritation or redness develops.

🤰 If Pregnant or Breast-Feeding 10 words ▾

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

📄 Keep Out of Reach of Children 20 words ▾

Keep out of reach of children If accidentally ingested, get medical help or contact a Poison Control Center right away.

📄 Other Information 8 words ▾

Other information Store in a cool, dry place.

📄 Questions or Comments 17 words ▾

Questions or Comments Call 1-832-709-0788 Monday through Friday 9 AM to 5 PM CST or visit www.richtofit.us.

📖 Instructions for Use ~1 min read ▾

Drug Facts Drug Facts Active Ingredients Menthol 5% – External Analgesic Camphor 4% – External Analgesic Warnings For external use only When using this product Use only as directed. Avoid contact with eyes or mucous membranes. Do not use on wounds, damaged, or irritated skin.

Do not bandage or use with a heating pad. Do not use if you are allergic to any of the ingredients. Do not use with other ointments, creams, or sprays.

Stop use and ask a doctor if condition worsens, symptoms persist for more than 7 days, or clear up and occur again within a few days, or irritation or redness develops. If pregnant or breast-feeding ask a health professional before use. Keep out of reach of children If accidentally ingested, get medical help or contact a Poison Control Center right away.

Directions Adults and children 2 years of age and older: apply to affected area not more than 4 times daily. Children under 2 years of age: ask a doctor. Other information Store in a cool, dry place.

Inactive Ingredients Water, Cetearyl Alcohol, Anthemis Nobilis Flower Oil, Chamomilla Recutita Flower Extract, Chamomilla Recutita Flower Oil, Humulus Lupulus Extract, Juglans Regia Leaf Extract, Lavandula Angustifolia Flower/Leaf/Stem Extract, Potentilla Anserina Extract, Quercus Robur Bark Extract, Salix Alba Bark Extract, Salvia Officinalis Leaf Extract, Glycerin, Cocos Nucifera Oil, Polysorbate 20, Phenoxyethanol, Fragrance, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Tocopherol, Sodium Hydroxide, Ethylhexylglycerin.

Questions or Comments Call 1-832-709-0788 Monday through Friday 9 AM to 5 PM CST or visit www.richtofit.us. use Temporary relief of minor aches and pains of muscles and joints associated with arthritis, simple backache, strains, sprains, and bruises. Purpose External Analgesic

📄 Package Label / Principal Display Panel ~1 min read ▾

PRINCIPAL DISPLAY PANEL CONTENTS RICHTOFIT RAPIDACTIVE ARTHRITIS GEL NDC 87384-058-10 Cooling Pain Relief Intensive Formula RapidActive Arthritis Gel Soothing and Revitalizing Non Greasy – Fast Acting Net Wt. 3 oz (85 g) Richtofit Complex Formula Herbal Extracts Made in U.S.A.

Descriptive Text RICHTOFIT RAPIDACTIVE ARTHRITIS GEL combines the fast-acting cooling power of Menthol and Camphor with the restorative effects of the Richtofit Herbal Complex, a European blend trusted for over 40 years. This smooth, non-greasy gel helps soothe the body by relieving minor muscle and joint aches, easing stiffness, and delivering a cooling sensation that refreshes tired, stressed areas. Herbal extracts including Chamomile, Lavender, Sage Leaf, Willow Bark, and Walnut Leaf help comfort the skin, soften rough areas, and support a naturally revitalized feel.

Ideal for daily use, before or after activity, or anytime the body needs cooling comfort. Temporary cooling relief of minor aches and pains. Soothes the body, easing tension and stressed areas.

Revitalizing herbal effects refresh tired muscles and joints, reducing stiffness. Herbal extracts help comfort and condition the skin. Provides both targeted pain relief and body comfort.

Manufacture Manufactured in U.S.A. for: Richtofit Limited Liability Company 611 Choctaw Lane, Suite G Katy, TX 77494 NDC 87384-058-10 Net Wt. 3 oz (85 g)

TUBE IMAGE RICHTOFIT RAPID ACTIVE ARTHRITIS GEL TUBE

BOX IMAGE RICHTOFIT RAPID ACTIVE ARTHRITIS GEL 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 RICHTOFIT LIMITED LIABILITY COMPANY. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
RICHTOFIT LIMITED LIABILITY COMPANY 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.
← 87383-0010-00 · Fidelio 87384-0059-10 · RICHTOFIT →
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.