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Ultra Strength Topical Pain Relief Cream Camphor, Menthol, Methyl Salicylate 100 mg/g; 300 mg/g; 40 mg/g Cream, 57 g — NDC 82729-0006-01 package photo

Ultra Strength Topical Pain Relief Cream Camphor, Menthol, Methyl Salicylate 100 mg/g; 300 mg/g; 40 mg/g Cream, 57 g

by J C UDEOZOR & SONS GLOBAL INDUSTRIES LTD · 57 g in 1 TUBE (82729-006-01)
NDC 82729-0006-01
🏷️ FDA NDC (as labeled) 82729-006-01 billing pads the product segment with a zero
OTC On market Non-controlled
🗂️ Data synced 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

FDA NDC (as labeled) 82729-006-01
Product NDC 82729-006
11-digit billing NDC 82729000601
RxCUI 283083
UNII BZ1R15MTK7, LAV5U5022Y, N20HL7Q941
Application # M017
SPL Set ID 4db9ae57-4ab4-8fe4-e063-6394a90a7e51
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-03-31
Route TOPICAL
Dosage form CREAM
Substance LEVOMENTHOL; METHYL SALICYLATE; CAMPHOR (NATURAL)
Why two NDCs? The FDA registers this code as 82729-006-01 — 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 → 82729-0006-01. 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.

🏭 Manufacturer & labeler

LabelerJ C UDEOZOR & SONS GLOBAL INDUSTRIES LTD
FDA applicationM017 (OTC MONOGRAPH DRUG)
Labeler code82729
First marketedMar 2026
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.

🩺 Clinical

🧪 What is this product?

This is an over-the-counter topical cream marketed under FDA's OTC monograph rules for pain relief products. It contains three active ingredients: camphor, menthol (levomenthol), and methyl salicylate, which are commonly combined in topical products to provide a warming or cooling sensation and to be typically used for temporary relief of minor muscle and joint aches. The cream is applied directly to the skin over the affected area.

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.

💊 What it looks like

Color white
FlavorMenthol
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 59TL3WG5CO
    A synthetic polymer made by crosslinking acrylic acid with allyl sucrose. It thickens liquids, forms gels, and helps control how fast the medicine is released in your body.
  • UNII 8NLQ36F6MM
    Edetate disodium anhydrous is a chemical compound that binds to metal ions in a medicine. It's used as a stabilizer to prevent unwanted chemical reactions and help keep the drug product effective during storage.
  • UNII 258491E1RZ
    A waxy substance made from glycerin and stearic acid, commonly used as an emulsifier to help blend oil and water ingredients together in medicines. It also helps thicken and stabilize the product's texture.
  • UNII 7EV65EAW6H
    Lanolin is a waxy substance derived from sheep's wool. It's used in medicines as an emollient and skin-conditioning agent to soften formulations and improve spreadability in topical products like creams and ointments.
  • UNII 6OZP39ZG8H
    Polysorbate 80 is a synthetic emulsifier derived from sorbitol and oleic acid. It helps mix oil and water-based ingredients together in medications and improves how the product disperses in the body.
  • UNII WZH3C48M4T
    Potassium hydroxide is a strong alkaline chemical used in medicines to adjust and maintain the pH level of liquid formulations, helping keep the product stable and the active ingredients effective.
  • UNII 4ELV7Z65AP
    Stearic acid is a fatty acid derived from plant or animal sources. It acts as a binder and lubricant in tablets and capsules, helping them hold together and flow smoothly during manufacturing.
  • 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.

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

The official label also statesCarbomer, Disodium EDTA, Glyceryl Stearate, Lanolin, Polysorbate 80, Potassium Hydroxide, Stearic Acid, Water

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.
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
Good Neighbor Muscle Rub Cream 100 mg/g; 40 mg/g; 300 mg/g 46122-0816-36 Amerisource 1 tube $0.036 — Availability likely —
Leader Ultra Strength Muscle Rub Topical Analgesic 40 mg/g; 100 mg/g; 300 mg/g 70000-0208-01 Cardinal 1 tube $0.036 — Availability likely —
Walgreens Pain Relieving Analgesic 40 mg/g; 100 mg/g; 300 mg/g 00363-1199-01 Walgreen 1 tube — — FDA listed —
Ultra Strength Muscle Rub 40 mg/g; 100 mg/g; 300 mg/g 10742-6000-01 The 1 tube — — FDA listed —
Rite Aid Muscle Rub Ultra Strength 40 mg/g; 100 mg/g; 300 mg/g 11822-7957-08 Rite 1 tube — — FDA listed —
Kroger Muscle Rub Cream 40 mg/g; 100 mg/g; 300 mg/g 30142-0427-02 Kroger 1 tube — — FDA listed —
AVON HeXashield Pain Relief for Muscle, Back and Joint Cream 100 mg/g; 300 mg/g; 40 mg/g 43136-0102-01 Tai 1 tube — — FDA listed —
Equate Pain Relieving Ultra Strength 40 mg/g; 100 mg/g; 300 mg/g 49035-0700-01 Wal-Mart 1 tube — — FDA listed —
XRay Pain Relief 100 mg/g; 40 mg/g; 300 mg/g 50066-0456-20 Genomma 1 tube — — FDA listed —
Pomada Dragon Pain Relief 100 mg/g; 40 mg/g; 300 mg/g 50066-0622-02 Genomma 1 tube — — FDA listed —
Ultra Strength Muscle Rub - CVS Health Ultra Strength Muscle Rub 40 mg/g; 300 mg/g; 100 mg/g 51316-0982-01 CVS 1 tube — — FDA listed —
Ultra Pain-A-Trate Pain-Relieving Cream 3.4 g/85g; 8.5 g/85g; 25.5 g/85g 54473-0334-03 Melaleuca, 85 g — — FDA listed —
Pomada Dragon Pain Relieving 40 mg/g; 100 mg/g; 300 mg/g 55038-0001-02 TELEVISA 1 tube — — FDA listed —
Family Wellness Ultra Strength Muscle Rub 40 mg/g; 100 mg/g; 300 mg/g 55319-0820-57 FAMILY 1 tube — — FDA listed —
Coolexa 40 mg/g; 100 mg/g; 300 mg/g 57237-0351-13 Rising 1 tube — — FDA listed —
CVS Health Muscle Rub Ultra Strength 40 mg/g; 100 mg/g; 300 mg/g 59779-0792-01 CVS 1 tube — — FDA listed —
Family Care Muscle Rub 40 mg/g; 100 mg/g; 300 mg/g 65923-0987-35 United 1 tube — — FDA listed —
Bengay Ultra Strength Non-Greasy 40 mg/g; 100 mg/g; 300 mg/g 69968-0538-02 Kenvue 1 tube — — FDA listed —
HealthWise Ultra OTC Strength Pain Relief Cream 40 mg/g; 100 mg/g; 300 mg/g 71101-0070-01 Veridian 1 tube — — FDA listed —
Meijer Ultra Strength Pain Relieving Topical Analgesic 40 mg/g; 100 mg/g; 300 mg/g 79481-1220-01 Meijer 1 tube — — FDA listed —
Ultra Strength Topical Pain Relief Cream 100 mg/g; 300 mg/g; 40 mg/gthis 82729-0006-01 J 57 g — — FDA listed —
Sync Pro 30 g/1; 4 g/1; 10 g 82944-0400-10 iON 1 tube — — FDA listed —
Care Lix Pain Relief 4 g/100g; 10 g/100g; 30 g/100g 87371-0001-01 ACQUIRED 57 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

🏛️
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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
82729-0006-01 You're viewing this 57 g in 1 TUBE (82729-006-01) 2026-03-31 Active

🧭 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 82729-006-01, 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: 82729-0006-01, written without dashes as 82729000601. 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 82729-0006-01, the first segment (82729) is the labeler code FDA assigned to J C UDEOZOR & SONS GLOBAL INDUSTRIES LTD; the middle segment (0006) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (01) 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 J C UDEOZOR & SONS GLOBAL INDUSTRIES LTD. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
J C UDEOZOR & SONS GLOBAL INDUSTRIES LTD 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 🎯 Purpose
🎯 Indications and Usage 21 words ▾

USES Temporarily relieves minor aches & pains related to: arthritis simple backaches sore muscles joint pain dislocation leg cramps bruises sprains

⏱️ Dosage and Administration 36 words ▾

Direction Use only as directed For adults and children over 12 years, apply to the affected area 3 to 4 times daily Wash hands after use For Children under 12 years, consult a doctor before use

⚠️ Warnings 5 words ▾

Warning For external use only.

🧪 Active Ingredient 14 words ▾

Active Ingredients Active Ingredients (In each gram) Camphor 4% Menthol 10% Methyl Salicylate 30%

🧪 Inactive Ingredients 15 words ▾

Inactive Ingredients Carbomer, Disodium EDTA, Glyceryl Stearate, Lanolin, Polysorbate 80, Potassium Hydroxide, Stearic Acid, Water

🎯 Purpose 21 words ▾

Purpose Active Ingredients (In each gram) ​ Purpose Camphor 4% External Analgesic Menthol 10% External Analgesic Methyl Salicylate 30% External Analgesic

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 82725-4202-01 · Cabinet 82730-0100-05 · Good →
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.