Deep Numbing Cream MENTHOL 10 g/100g Cream
by YITONGBADA (SHENZHEN) INTERNATIONAL TRADE CO., LTD · 1 BOTTLE in 1 BOX (83364-023-01) / 60 g in 1 BOTTLE
NDC 83364-0023-01
🏷️ FDA NDC (as labeled)
83364-023-01
billing pads the product segment with a zero
OTC
On market
Non-controlled
🗂️ Data synced Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →
⚠️
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
FDA NDC (as labeled)
83364-023-01
Product NDC
83364-023
11-digit billing NDC
83364002301
RxCUI
253020
UNII
L7T10EIP3A
UPC
0810169303016
Application #
M017
SPL Set ID
7943559b-de10-4214-96dc-f9cbac828f46
DEA schedule
Non-controlled
Marketing category
OTC MONOGRAPH DRUG
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
2026-04-13
Route
TOPICAL
Dosage form
CREAM
Substance
MENTHOL
Why two NDCs?
The FDA registers this code as 83364-023-01 — 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 → 83364-0023-01. 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
LabelerYITONGBADA (SHENZHEN) INTERNATIONAL TRADE CO., LTD
FDA applicationM017 (OTC MONOGRAPH DRUG)
Labeler code83364
First marketedApr 2026
Product typeHuman Otc Drug
Portfolio6 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.
🩺 Clinical
📗 Our plain-language guide HelloPharmacist
- Menthol is found in a lot of over-the-counter topical products — creams, gels, patches, sprays, and powders. Depending on the product, it's used to temporarily ease minor muscle an...
- Start with clean, dry skin — free of lotions or creams — before applying the patch. Peel the backing off and press the sticky side firmly to the sore area. Most menthol patches sho...
- Yes, a mild burning or tingling feeling right after applying a menthol product is common and usually settles down within a few days of regular use. What's not normal is severe burn...
- Is that burning sensation after I apply it normal?
Patient education
Supplement & herbal interactions
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.
💬 Questions about MENTHOL?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
🧪 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.
💲 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 system | Per g | Per 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
| Product | Labeler | Pack | NADAC/unit | TE | Status | Price vs. this |
|---|---|---|---|---|---|---|
| Walgreens Cold Therapy Pain Relief Foot Cream 100 mg/g 00363-1292-04 | Walgreen | 113 g | — | — | FDA listed | — |
| Menthol Pain Relieving Cream with Menthol 10% .1 g/g 55629-0018-05 | ONE2ZEE | 141 g | — | — | FDA listed | — |
| Biofreeze Foot Cream 100 mg/g 59316-0001-10 | Reckitt | 85 g | — | — | FDA listed | — |
| Biofreeze Foot Pain Relief Set 59316-0002-10 | Reckitt | 1 kit | — | — | FDA listed | — |
| Biofreeze 100 mg/g 59316-0869-10 | Reckitt | 85 g | — | — | FDA listed | — |
| Biofreeze 100 mg/g 59316-0870-10 | Reckitt | 85 g | — | — | FDA listed | — |
| PROINNATE Numbing Cream 10 g/100g 60771-0024-01 | Guangzhou | 120 g | — | — | FDA listed | — |
| PROINNATE Numbing Cream 10 g/100g 60771-0039-01 | Guangzhou | 30 g | — | — | FDA listed | — |
| CVS Health Pain Relief Foot 100 mg/g 66902-0292-04 | NATURAL | 113 g | — | — | FDA listed | — |
| HealthWise Pain Relieving Cream 10 g/100g 71101-0075-01 | Veridian | 1 jar | — | — | FDA listed | — |
| HealthWise Pain Relieving Cream Lavender 10 g/100g 71101-0076-01 | Veridian | 1 jar | — | — | FDA listed | — |
| Debbies Down and Dirty Deep Tissue Joint and Muscle 100 mg/mL 71523-0833-01 | DD&D | 1 bottle | — | — | FDA listed | — |
| Relieve Your Pain 10 g/100g 72683-0005-01 | Proximity | 96 g | — | — | FDA listed | — |
| KINETIC ICE Muscle and Joint Pain Relief Cream 100 mg/mL 81050-0108-00 | No | 118 ml | — | — | FDA listed | — |
| Deep Numbing Cream 10 g/100gthis 83364-0023-01 | YITONGBADA | 1 bottle | — | — | FDA listed | — |
| The Body Builders Cream 100 mg/mL 87282-0912-00 | Smart | 100.6 ml | — | — | FDA listed | — |
| Joint and Muscle Relief Topical Analgesic 100 mg/mL 87282-0988-00 | Smart | 100.6 ml | — | — | FDA listed | — |
| Deep Blue Copaiba 10 g/100g 71630-0169-48 | doTERRA | 48 g | — | — | Discontinued | — |
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
Apr 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.
🔬 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 Deep Numbing Cream (this brand).
Top reported reactions
Age at onset
Reporter sex
Serious outcomes
Reports over time (by year) — tap or hover for the count & year
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.
📦 Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Status |
|---|---|---|---|
| 83364-0023-01 You're viewing this | 1 BOTTLE in 1 BOX (83364-023-01) / 60 g in 1 BOTTLE | 2026-04-13 | 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) | — 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 FDA registers it as 83364-023-01, 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: 83364-0023-01, written without dashes as 83364002301. 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 83364-0023-01, the first segment (83364) is the labeler code FDA assigned to YITONGBADA (SHENZHEN) INTERNATIONAL TRADE CO., LTD; the middle segment (0023) 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 YITONGBADA (SHENZHEN) INTERNATIONAL TRADE CO., LTD. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
YITONGBADA (SHENZHEN) INTERNATIONAL 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.
📄 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 ▾
Uses ■ For the temporary relief of localized pain, itching, or discomfort from minor skin irritations. When using this product ■ Avoid contact with eyes ■ Do not exceed the recommended daily dosage unless directed by a doctor. ■ Do not put this product into the rectum by using fingers or any mechanical device or applicator. Stop use and ask a doctor if ■ Condition worsens or does not improve within 7 days. ■ An allergic reaction occurs to ingredients in this product. ■ Redness, irritation, swelling, pain, or other symptoms develop or increase. ■ Symptoms clear up and occur again within a few days.
Keep out of reach of children. In case of accidental ingestion, seek medical advice immediately or contact a Poison Control Center right away. If pregnant or breastfeeding, ask a health professional before use.
⏱️ Dosage and Administration ▾
Directions ■ When practical, cleanse the affected area with mild soap and warm water, then rinse thoroughly. ■ Gently dry by patting or blotting with toilet tissue or a soft cloth before applying. ■ Adults and children 12 years and older: Apply externally to the affected area up to 6 times a day. ■ Children under 12 years of age: Consult a doctor.
⚠️ Warnings ▾
Warnings For external use only
🧪 Active Ingredient ▾
Active ingredients Menthol 10%
🧪 Inactive Ingredients ▾
Inactive ingredients Aqua, Arnica Montana Flower Extract, Ethylhexyl Palmitate, Glycerin, Propylene Glycol, Cetearyl Alcohol, Emu Oil, Soy Lecithin, Butyrospermum Parkii (Shea Oil), Alpha-Tocopherol Acetate, Zanthoxylum Bungeanum Fruit Extract, Daphne Feddei Extract, Paeonol, Curcuma Longa (Turmeric) Fruit Extract, Salvia Miltiorrhiza Root Extract, Dendrobium Officinale Stem Extract, Stephania Tetrandra Extract, Aesculus Hippocastanum (Horse Chestnut) Extract, Glycyrrhiza Glabra (Licorice) Root Extract
🎯 Purpose ▾
Purpose Topical Anesthetic
No label section mentions that — try another word, or open the full label on DailyMed below.
Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA.
Prefer the government’s original formatting? View this label on DailyMed ↗
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.