Home › NDC Lookup › Ingredients › Menthol › 83602-0323-30
🧴image loading
(from DailyMed)

Menthol Pain Relief Gel-Tube .04 g/mL Gel, 89 mL — NDC 83602-323-30 (Billing 83602-0323-30)

by Guangzhou Liuquanmiao Import & Export Trade Co., Ltd. · 89 mL in 1 TUBE

This is a package of 89 mL of Menthol Pain Relief Gel-Tube .04 g/mL Gel from Guangzhou Liuquanmiao Import & Export Trade Co., Ltd., marketed since Dec 2023 and currently FDA-listed. It is this product's only package size.

NDC 83602-0323-30
🏷️ FDA NDC (as labeled) 83602-323-30 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 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

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 83602-323-30
Product NDC 83602-323
11-digit billing NDC 83602032330
RxCUI 415974
UNII L7T10EIP3A
UPC 6974817678308, 6974817678315
Application # M017
SPL Set ID 0bb07892-824e-8691-e063-6294a90a3891
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2023-12-06
Route TOPICAL
Dosage form GEL
Substance MENTHOL
Quick answers
  • RxCUI (RxNorm): 415974
Why two NDCs? The FDA registers this code as 83602-323-30 — 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 → 83602-0323-30. 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.
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
83602-0323-30 You're viewing this Main listing 89 mL in 1 TUBE 2023-12-06 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Leader Cooling Pain Relief Topical Analgesic 40 mg/mL 70000-0618-01 Cardinal 89 ml $0.052 — Availability likely —
Leader Roll-On Cooling Pain Relief Topical Analgesic 40 mg/mL 70000-0617-01 Cardinal 74 ml $0.059 — Availability likely —
Gel Cooling Pain Relief 40 mg/mL 11344-0894-18 Nice-Pak 74 ml — — FDA listed —
Target Up and Up Pain Relief Menthol Topical Analgesic Roll-On 40 mg/mL 11673-0261-03 TARGET 89 ml — — FDA listed —
Gel Cooling Pain Relief 40 mg/mL 30142-0043-18 The 74 ml — — FDA listed —
TopCare Pain Relieving Roll-On Topical Analgesic 40 mg/mL 36800-0290-01 Topco 74 ml — — FDA listed —
4% Menthol PAIN RELIEF 4 g/100mL 43473-0095-25 Nantong 74 ml — — FDA listed —
4% Menthol Cold Therapy 4 g/100g 43473-0098-15 Nantong 1 tube — — FDA listed —
Dragon with Arnical Pain Relief 4 g/100g 50066-0621-56 Genomma 1 tube — — FDA listed —
Biofreeze Roll-On 40 mg/mL 50090-6358-00 A-S 74 ml — — FDA listed —
Biofreeze Colorless 40 mg/mL 50090-6361-00 A-S 89 ml — — FDA listed —
GoodSense Cooling Pain Relief 4 g/100mL 50804-0297-03 Geiss, 1 tube — — FDA listed —
CVS Pain Relief Lavender Scent 4 g/100mL 51316-0118-02 CVS 74 ml — — FDA listed —
CVS Pain Relief 4 g/100mL 51316-0161-02 CVS 74 ml — — FDA listed —
CVS Pain Relief 40 mg/mL 51316-0933-03 CVS 89 ml — — FDA listed —
CVS Pain Relief 4 g/100g 51316-0997-04 CVS 85 g — — FDA listed —
4% Menthol PAIN RELIEF 4 g/100mL 52000-0439-25 Universal 74 ml — — FDA listed —
4% Menthol Cold Therapy 4 g/100g 52000-0442-15 Universal 1 tube — — FDA listed —
DG Health Cold Zone Pain Relieving Topical Analgesic 40 mg/mL 55910-0884-01 Dolgencorp 59 ml — — FDA listed —
Biofreeze 40 mg/mL 59316-0102-10 Reckitt 5 ml — — FDA listed —
Biofreeze Colorless 40 mg/mL 59316-0103-12 Reckitt 89 ml — — FDA listed —
Biofreeze Overnight Gel 40 mg/mL 59316-0121-10 Reckitt 89 ml — — FDA listed —
Biofreeze Roll-On 40 mg/mL 59316-0205-10 Reckitt 89 ml — — FDA listed —
Biofreeze Colorless Roll-On 40 mg/mL 59316-0206-10 Reckitt 1 bottle — — FDA listed —
Biofreeze Overnight Roll-on 40 mg/mL 59316-0207-14 Reckitt 74 ml — — FDA listed —
Biofreeze Roll-On and Overnight Roll-On 59316-0209-14 Reckitt 2 bottles — — FDA listed —
Pain Relieving 4 g/100g 61010-4403-01 Safetec 113.4 g — — FDA listed —
X-Treme Freeze 4 g/100mL 67777-0144-10 Dynarex 100 packets — — FDA listed —
Cold Therapy Roll on .04 g/mL 69168-0483-67 Allegiant 74 ml — — FDA listed —
Pain Relief Gel Roll On 40 g/L 69396-0184-01 Trifecta 1 bottle — — FDA listed —
Tommie Copper Cooling Roller Lavender Scent 4 g/100mL 72562-0185-03 Tommie 89 ml — — FDA listed —
DCH Cooling Pain Relief 4 g/100mL 72839-0297-03 Derma 89 ml — — FDA listed —
PAIN RELIEF Gel-Tube .04 g/mL 73557-0323-30 Shanghai 89 ml — — FDA listed —
PAIN RELIEF Gel-Roll On .04 g/mL 73557-0333-25 Shanghai 74 ml — — FDA listed —
BonicaEaseX Colorless Roll-On Menthol Pain Relieving 40 mg/mL 75568-0041-00 Planet 3 bottles — — FDA listed —
BonicaEaseX Menthol Pain Relieving 40 mg/mL 75568-0043-00 Planet 3 tubes — — FDA listed —
Gel Cooling Pain Relief 40 mg/mL 76162-0894-21 Topco 89 ml — — FDA listed —
meijer Cold Therapy Pain Relieving analgesic 40 mg/mL 79481-0087-01 Meijer 89 ml — — FDA listed —
meijer ROLL-ON Cold Therapy Pain Relieving Topical analgesic 40 mg/mL 79481-0088-01 Meijer 74 ml — — FDA listed —
Equate Cold Therapy Pain Relieving Analgesic 40 mg/mL 79903-0021-01 Wal-Mart 89 ml — — FDA listed —
Equate Cold Therapy Pain Relieving Roll-on Analgesic 40 mg/mL 79903-0022-01 Wal-Mart 74 ml — — FDA listed —
Thera Plus Cold Therapy Pain Relieving Menthol 40 mg/mL 80684-0101-00 Fourstar 74 ml — — FDA listed —
Sync Ice 4 g 82944-0300-74 iON 1 bottle — — FDA listed —
DIRT Pain Relieving Gel 40 mg/mL 83067-0363-00 PURIVITAE, 88 ml — — FDA listed —
DIRT Pain Relieving Gel 40 mg/mL 83067-0463-00 PURIVITAE, 88 ml — — FDA listed —
Quality Choice Cold Therapy Gel 40 mg/mL 83324-0007-04 Chain 118.2 ml — — FDA listed —
Auvon 4% Menthol Pain Relief Gel .04 mg/mL 83391-0007-01 SHENZHEN 89 ml — — FDA listed —
Menthol Pain Relief Gel-Tube .04 g/mLthis 83602-0323-30 Guangzhou 89 ml — — FDA listed —
Menthol Pain Relief Gel-Roll On .04 g/mL 83602-0333-25 Guangzhou 74 ml — — FDA listed —
Pain Relief Gel-Tube .04 g/mL 84008-0003-02 Bullet 1 bottle — — FDA listed —
Cold Hot Chinese Red Tiger Pain Relief Gel Roll-On 4 g/100mL 84165-0008-01 Guangzhou 1 bottle — — FDA listed —
Plantar Fasciitis Chinese Red Tiger Pain Relief Gel Roll-On 4 g/100mL 84165-0009-01 Guangzhou 1 bottle — — FDA listed —
HEEL PAIN Relief Gel Roll-On .04 g/mL 84165-0011-01 Guangzhou 1 bottle — — FDA listed —
PLANTAR FASCIITIS Relief Gel Roll-On 4 g/100mL 84165-0012-01 Guangzhou 1 bottle — — FDA listed —
PRO COLD HOT Pain Relief Gel Roll-On (Plantar Fasciitis) 4 g/100mL 84165-0013-01 Guangzhou 1 bottle — — FDA listed —
AVCOO Pain Relief 4 g/100mL 84992-0003-01 ADP 89 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

🏛️
2023
On the market since
Dec 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.

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.

Loading inactive ingredients from the official FDA label in the background. No external source is being called by this page request.
Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.

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

LabelerGuangzhou Liuquanmiao Import & Export Trade Co., Ltd.
FDA applicationM017 (OTC MONOGRAPH DRUG)
Labeler code83602
First marketedDec 2023
Product typeHuman Otc Drug
Portfolio20 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 📄 Ask a Doctor Before Use If 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 🤰 If Pregnant or Breast-Feeding 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 19 words ▾

Uses Temporarily relieves muscle soreness and minor joint pains in the wrist, knees, ankle, back, neck, hips, shoulders, elbows.

⏱️ Dosage and Administration 43 words ▾

Directions Adults and children 12 years of age and older: • Rub a thin film over affected areas not more than 4 times daily; • Message not necessary Children under 12 years of age: Consult physician. Wash hands after use with cool water.

⚠️ Warnings 5 words ▾

Warnings For external use only

🧪 Active Ingredient 8 words ▾

Active ingredient Menthol 4% ...... Purpose: Topical Analgesic

🧪 Inactive Ingredients 39 words ▾

Inactive ingredients Alcohol, Aloe Barbadensis Leaf Extract, Arnica Montana Flower Extract, Boswellia Carterii Resin Extract, Camellia Sinensis Leaf Extract, Carbomer, Camphor, FD&C Blue 1, FD&C Yellow 5, Glycerin, Isopropyl Myristate, Ilex Paraguariensis Leaf Extract, Silica, Triethanolamine, Vitamin E, Water

🎯 Purpose 3 words ▾

Purpose Topical Analgesic

📄 Do Not Use 35 words ▾

Do not use • on wounds or damaged skin • with a heating pad or device • with other ointments, creams, sprays, or liniments • if you are allergic to any ingredients of this product

📄 Ask a Doctor Before Use If 25 words ▾

... ask a doctor if • skin reactions such as redness, swelling, blistering or other discomfort occur • symptoms persist for more than 7 days

📄 When Using This Product 24 words ▾

When using this product • use only as directed • avoid contact with the eyes, mucous membranes, or rashes • do not bandage tightly

📄 Stop Use and Ask a Doctor If 24 words ▾

Stop use ... if • skin reactions such as redness, swelling, blistering or other discomfort occur • symptoms persist for more than 7 days

🤰 If Pregnant or Breast-Feeding 10 words ▾

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

📄 Keep Out of Reach of Children 19 words ▾

KEEP OUT OF REACH OF CHILDREN. If swallowed accidentally, get medical help or contact with Poison Control Center immediately.

📄 Questions or Comments 5 words ▾

Questions or Comments: [email protected] patch

📄 Package Label / Principal Display Panel 1 words ▾

30

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 Menthol Pain Relief Gel-Tube (this brand).

Top reported reactions

Dyspnoea85
Fatigue84
Pain81
Pruritus78
Dizziness67
Headache67
Cough65

Reporter sex

989 reports

Serious outcomes

Death125
Disabling26
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 109 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 — Not published for this NDC No photo available yet for this listing.
Inactive ingredients (structured) — Not published for this NDC The labeler did not submit a structured excipient list, or no SPL is 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 Guangzhou Liuquanmiao Import & Export Trade Co., Ltd.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Guangzhou Liuquanmiao Import & Export Trade Co., 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.
← 83602-0311-36 · Guangzhou 83602-0333-25 · Guangzhou →
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.