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MIND BODY MATRIX PAIN RELIEF MENTHOL 15 mg/mL Cream — NDC 72268-0175-10 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

MIND BODY MATRIX PAIN RELIEF MENTHOL 15 mg/mL Cream — NDC 72268-175-10 (Billing 72268-0175-10)

by Functional Energetic, Inc. · 1 JUG in 1 CARTON / 3840 mL in 1 JUG

This is a package of MIND BODY MATRIX PAIN RELIEF MENTHOL 15 mg/mL Cream from Functional Energetic, Inc., no longer marketed (first marketed Apr 2018), no longer in the FDA NDC Directory.

NDC 72268-0175-10
🏷️ FDA NDC (as labeled) 72268-175-10 billing pads the product segment with a zero
This package
Contains3840 mL in 1 jug Pack sizes3 compare ↓
Product page 72268-0175-01 Also comes in: 30 mL 72268-175-01 120 mL 72268-175-04
OTC Discontinued Non-controlled ⚠ Discontinued by firm ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed 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

NDC database record

One package, one record: these facts belong to NDC 72268-175-10 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
72268 labeler · 175 product · 10 package
Listing certified through
Dec 31, 2026
Barcode (UPC)
0853289008010
FDA record last changed
Jul 24, 2026
⚠️
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 ↗
⚠️
Excluded from the active FDA NDC Directory. The labeler reported this product as discontinued, so it is excluded from the active NDC Directory. A label may still appear on DailyMed, but the NDC is no longer in the current FDA NDC Directory. Search the FDA NDC Directory ↗

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 72268-175-10
Product NDC 72268-175
11-digit billing NDC 72268017510
RxCUI 1045482
UNII L7T10EIP3A
UPC 0853289008010
Application # M017
SPL Set ID 3667dd0d-942e-4101-ba98-cb013ae77cf5
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status Discontinued
FDA listing status Discontinued by firm
Marketing start 2018-04-20
Route TOPICAL
Dosage form CREAM
Substance MENTHOL
Quick answers
  • RxCUI (RxNorm): 1045482
Why two NDCs? The FDA registers this code as 72268-175-10 — 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 → 72268-0175-10. 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

📗 Our plain-language guide HelloPharmacist
  • Mostly for temporary relief of minor aches and pains in muscles and joints, like those from arthritis, backache, strains, sprains and bruises. Some products are for other things, s...
  • It depends on the product. Many creams, gels and patches are limited to about 3 to 4 times a day, and patches also have a time limit, often 8 hours. Follow your product label and a...
  • A brief burning feeling can happen when you first apply it and usually fades in several days. But if you get severe burning pain, swelling or blistering, stop using it and call you...
  • No. Don't use menthol products with a heating pad, and avoid local heat or direct sunlight on the area. Rare cases of serious burns have been reported.
📖 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.

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: 30 mL 120 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
72268-0175-01 72268-175-01 Main listing 1 TUBE in 1 BOX / 30 mL in 1 TUBE 2018-04-20 — Active
72268-0175-04 72268-175-04 1 TUBE in 1 BOX / 120 mL in 1 TUBE 2018-04-20 — Discontinued by firm
72268-0175-10 You're viewing this 1 JUG in 1 CARTON / 3840 mL in 1 JUG 2018-04-20 — Discontinued by firm

Pack size FAQ

What quantity is in this package?
This package is listed by the FDA — 1 jug in 1 carton / 3840 ml in 1 jug.
What NDC number is used to bill for this package of MIND BODY MATRIX PAIN RELIEF MENTHOL 15 mg/mL Cream?
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
4Jointz 1.5 g/100g 71282-0022-27 ARP(USA) 2 tubes — — FDA listed —
Mind Body Matrix Pain Relief 15 mg/mLthis 72268-0175-10 Functional 1 jug — — Discontinued —
ARTHRO LIFE Instant Pain Relief Cream 15 mg/mL 82986-0361-00 BIOBEST 59.15 ml — — FDA listed —
Dzul Arthritis Pain Relief 1.5 g/100g 83037-0015-04 Caball 114 g — — FDA listed —
PARACTIN QuantumActiv Pain Relief Cream 15 mg/mL 83224-0372-00 NHR 59.15 ml — — FDA listed —
Real Time Pain Relief Foot 15 mg/g 84573-0515-04 Real 125 g — — FDA listed —
Richtofit Rapid Active Leg And Foot 1.5 g/100g 87384-0059-10 RICHTOFIT 1 tube — — FDA listed —
Real Time Pain Relief Maxx Topical Analgesic 15 mg/mL 84573-0517-03 REAL 88 ml — — 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

🏛️
2018
On the market since
Apr 2018
📍
2026
Currently FDA-listed
8 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.

🧪 Avoiding an ingredient? See Menthol inactive ingredients by manufacturer: every current product's list side by side, so you can ask your pharmacy for the version that does not list it.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • UNII ZY81Z83H0X
    Aloe vera leaf is a plant extract derived from the aloe plant. It is used in medicines as a natural moisturizer and skin-soothing agent in topical formulations.
  • 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 P0M7O4Y7YD
    A plant extract from calendula flowers, traditionally used in formulations. It typically serves as a botanical ingredient that may provide color, fragrance, or skin-conditioning properties to topical products.
  • UNII 58B69Q84JO
    A plant-derived emulsifier made from olive oil and fatty alcohols. It helps blend oil and water ingredients together and stabilizes the product's texture in creams, lotions, and similar formulations.
  • UNII 936JST6JCN
    Cetyl alcohol is a waxy, fatty substance derived from plant or animal sources. It acts as an emulsifier and thickener in medicines, helping blend oil and water components and giving products a smooth, creamy texture.
  • UNII FGL3685T2X
    Chamomile is a plant extract used in medications as a flavoring agent and for its mild soothing properties in formulations. It helps improve taste and aroma of the medicine.
  • UNII 0N8672707O
    A starch derived from corn kernels. It acts as a binder to hold tablet ingredients together, a filler to give the tablet bulk, and a disintegrant to help the tablet break apart in your stomach.
  • UNII 9H4PO4Z4FT
    A sulfur-containing organic compound used as a solvent and penetration enhancer in medicines. It helps dissolve active ingredients and improve their absorption through skin or mucous membranes.
  • UNII WQ29KQ9POT
    Gluconolactone is a mild organic acid derived from glucose. It functions as a buffer and pH regulator in medicines, helping maintain stable acidity levels and improve product stability.
  • 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 WH8T92A065
    A fatty acid derivative made by combining stearic acid with glycerin and citric acid. It acts as an emulsifier to help mix oil and water-based ingredients, and also serves as a thickener in the medicine formulation.
  • UNII BKJ0J3D1BP
    A plant-derived ingredient from sunflower flowers, used as a natural colorant and flavoring agent in medicines. It may help provide color or mild taste to the product.
  • UNII 4PW41QCO2M
    Indian frankincense is a natural resin extracted from trees native to India. It is used in medicines as a binder and thickening agent to help hold ingredients together and improve texture.
  • UNII ZBP1YXW0H8
    A fragrant oil extracted from lavender plants, used as a flavoring and scent agent in medicines to improve taste and aroma.
  • UNII G43C57162K
    A natural plant extract from tea tree leaves used in topical formulations. It acts as a fragrance, preservative, and antimicrobial agent to help maintain product freshness and sensory appeal.
  • UNII LAV5U5022Y
    Methyl salicylate is a naturally derived liquid compound commonly found in wintergreen plants. In medicines, it's used as a flavoring agent and penetrating solvent to help distribute active ingredients evenly throughout topical products.
  • 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 ETJ7Z6XBU4
    Silicon dioxide is a naturally occurring mineral used as a glidant and anti-caking agent. It helps powder ingredients flow smoothly and prevents clumping during manufacturing and storage.
  • UNII OJ245FE5EU
    Sodium benzoate is a salt derived from benzoic acid, a preservative. It's added to medicines to prevent growth of bacteria, fungi, and other microorganisms that could spoil the product.
  • UNII MDL271E3GR
    Sorbitan olivate is an emulsifier derived from sorbitol and olive oil. It helps blend water and oil ingredients together to maintain consistent texture and appearance throughout the medicine.
  • UNII 24SC3U704I
    A powdery carbohydrate extracted from tapioca plant roots. It acts as a binder to hold tablet ingredients together and as a disintegrant to help the tablet break apart in your digestive system.
  • UNII 8021PR16QO
    Theanine is an amino acid found naturally in tea leaves. In medications, it's typically used as an active ingredient for its potential calming effects, though it may also function as a flavor component or dietary supplement ingredient in some formulations.
  • 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.
  • UNII TTV12P4NEE
    Xanthan gum is a thickening and stabilizing ingredient made from fermented corn or other sugars. It's added to medicines to improve texture, prevent separation of liquids and solids, and help the product stay consistent.

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

The official label also statesALOE BARBADENSIS (ALOE VERA GEL) JUICE, AQUA (DEIONIZED WATER), ARNICA MONTANA FLOWER EXTRACT, BOSWELLIA SERRATA EXTRACT, CALENDULA 0FFICINALIS EXTRACT, CETEARYL OLIVATE, CETYL ALCOHOL, CHAMOMILLA RECUTITA (CHAMOMILE) EXTRACT, CITRUS LIMONUM MEDICA (LEMON BALM) EXTRACT, G-AMINOBUTYRIC ACID, GLUCONOLACTONE, GLYCERIN, GLYCERYL STEARATE, HELIANTHUS ANNUUS (SUNFLOWER) OIL, LAVANDULA ANGUSTIFOLIA (LAVENDER) OIL, LECITHIN, MELALEUCA ALTERNIFOLIA (TEA TREE) OIL, MENTHA PIPERITA (PEPPERMINT) OIL, METHYL SALICYLATE (WINTERGREEN) OIL, METHYLSULFONYLMETHANE (MSM), SILICA, SODIUM BENZOATE, SORBITAN OLIVATE, TAPIOCA STARCH, L-THEANINE, XANTHAN GUM, ZEMEA (CORN) PROPANEDIOL.

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

LabelerFunctional Energetic, Inc.
FDA applicationM017 (OTC MONOGRAPH DRUG)
Labeler code72268
First marketedApr 2018
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 🎯 Purpose 📄 Do Not Use 🤰 If Pregnant or Breast-Feeding 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 24 words ▾

INDICATIONS: FOR THE TEMPORARY RELIEF OF MINOR ACHES AND PAINS OF THE MUSCLES AND JOINTS ASSOCIATED WITH ARTHRITIS, SIMPLE BACKACHE, SPRAINS, BRUISES AND STRAINS.

⏱️ Dosage and Administration 29 words ▾

DIRECTIONS: ADULTS AND CHILDREN TWO-YEARS OF AGE OR OLDER: APPLY TO AFFECTED AREA NOT MORE THAN THREE TO FOUR TIMES DAILY. CHILDREN UNDER TWO-YEARS OF AGE: CONSULT A PHYSICIAN.

⚠️ Warnings 54 words ▾

WARNINGS: FOR EXTERNAL USE ONLY. AVOID CONTACT WITH EYES. IF SYMPTOMS PERSIST FOR MORE THAN SEVEN DAYS, DISCONTINUE USE AND CONSULT PHYSICIAN. KEEP OUT OF REACH OF CHILDREN. IF SWALLOWED, CONSULT PHYSICIAN DO NOT APPLY TO WOUNDS OR DAMAGED SKIN. DO NOT BANDAGE TIGHTLY. IF PREGNANT OR BREAST FEEDING, CONTACT PHYSICIAN PRIOR TO USE.

🧪 Active Ingredient 6 words ▾

ACTIVE INGREDIENT: MENTHOL 1.50% TOPICAL ANALGESIC

🧪 Inactive Ingredients 78 words ▾

OTHER INGREDIENTS: ALOE BARBADENSIS (ALOE VERA GEL) JUICE, AQUA (DEIONIZED WATER), ARNICA MONTANA FLOWER EXTRACT, BOSWELLIA SERRATA EXTRACT, CALENDULA 0FFICINALIS EXTRACT, CETEARYL OLIVATE, CETYL ALCOHOL, CHAMOMILLA RECUTITA (CHAMOMILE) EXTRACT, CITRUS LIMONUM MEDICA (LEMON BALM) EXTRACT, G-AMINOBUTYRIC ACID, GLUCONOLACTONE, GLYCERIN, GLYCERYL STEARATE, HELIANTHUS ANNUUS (SUNFLOWER) OIL, LAVANDULA ANGUSTIFOLIA (LAVENDER) OIL, LECITHIN, MELALEUCA ALTERNIFOLIA (TEA TREE) OIL, MENTHA PIPERITA (PEPPERMINT) OIL, METHYL SALICYLATE (WINTERGREEN) OIL, METHYLSULFONYLMETHANE (MSM), SILICA, SODIUM BENZOATE, SORBITAN OLIVATE, TAPIOCA STARCH, L-THEANINE, XANTHAN GUM, ZEMEA (CORN) PROPANEDIOL.

🎯 Purpose 2 words ▾

TOPICAL ANALGESIC

📄 Do Not Use 12 words ▾

DO NOT APPLY TO WOUNDS OR DAMAGED SKIN. DO NOT BANDAGE TIGHTLY.

🤰 If Pregnant or Breast-Feeding 10 words ▾

IF PREGNANT OR BREAST FEEDING, CONTACT PHYSICIAN PRIOR TO USE.

📄 Keep Out of Reach of Children 10 words ▾

KEEP OUT OF REACH OF CHILDREN. IF SWALLOWED, CONSULT PHYSICIAN

📄 Package Label / Principal Display Panel 3 words ▾

Package Labeling: Label

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 No longer marketed (per FDA listing data)
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.
What does the discontinued status mean for this NDC?
The labeler reported a marketing end date (or the listing was delisted), so this specific package is no longer actively marketed. Remaining stock may still be dispensed for a time, and the NDC stays valid for historical records and claims — but data feeds (pricing, labeling) typically stop updating for it. Other package sizes or other manufacturers' versions of the same medication may still be marketed — see the equivalents section where available.
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.
Does this product come in other package sizes?
Yes — the FDA directory lists 2 other package presentations of this same product, including 1 tube (72268-0175-01), 1 tube (72268-0175-04). 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?
Functional Energetic, Inc. 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.
← 72266-0269-10 · Fosun 72273-0364-01 · Horizon →
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.