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TIDL PAIN RELIEF CRYO THERAPY original formula Spray. 10.5 g/100mL Spray, 90 mL — NDC 84214-0001-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

TIDL PAIN RELIEF CRYO THERAPY original formula Spray. 10.5 g/100mL Spray, 90 mL — NDC 84214-001-01 (Billing 84214-0001-01)

by Shenzhen Sam Technology Co., Ltd. · 90 mL in 1 BOTTLE, SPRAY

This is a package of 90 mL of TIDL PAIN RELIEF CRYO THERAPY original formula Spray. 10.5 g/100mL Spray from Shenzhen Sam Technology Co., Ltd., marketed since Jul 2024 and currently FDA-listed. It is this product's only package size.

NDC 84214-0001-01
🏷️ FDA NDC (as labeled) 84214-001-01 billing pads the product segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 8, 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 84214-001-01 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
84214 labeler · 001 product · 01 package
Package marketed since
Jul 12, 2024
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC)
0850020158386
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 84214-001-01
Product NDC 84214-001
11-digit billing NDC 84214000101
RxCUI 1489073
UNII L7T10EIP3A
UPC 0850020158386
Application # M017
SPL Set ID 1d0b94ec-f956-dff2-e063-6294a90aca4a
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2024-07-12
Route TOPICAL
Dosage form SPRAY
Substance MENTHOL
Quick answers
  • RxCUI (RxNorm): 1489073
Why two NDCs? The FDA registers this code as 84214-001-01 — 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 → 84214-0001-01. 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.

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 mLPer 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
84214-0001-01 You're viewing this Main listing 90 mL in 1 BOTTLE, SPRAY 2024-07-12 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Cold Therapy Pain Relief Walgreens 10.5 g/100g 00363-4411-85 WALGREEN 85 g — — FDA listed —
Rite Aid Cooling Pain Relief 10.5 g/100g 11822-0639-03 Rite 85 g — — FDA listed —
CVS Pain Relief 10.5 g/100g 51316-0996-10 CVS 85 g — — FDA listed —
Biofreeze 105 mg/mL 59316-0114-10 Reckitt 89 ml — — FDA listed —
Biofreeze Professional 105 mg/mL 59316-0120-20 Reckitt 118 ml — — FDA listed —
Biofreeze 105 mg/mL 59316-0833-10 Reckitt 89 ml — — FDA listed —
Biofreeze Professional 105 mg/mL 59316-0834-20 Reckitt 118 ml — — FDA listed —
Pain Relief 10.5 g/100mL 69396-0175-03 Trifecta 89 ml — — FDA listed —
GuruNanda Pain Relief 105 mg/mL 70708-0834-02 GURUNANDA, 1 bottle — — FDA listed —
DCH Cooling Pain Relief 10.5 g/100g 72839-0639-03 Derma 85 g — — FDA listed —
Meijer Pain Relief 10.5 g/100g 79481-0639-03 Meijer 85 g — — FDA listed —
Equate Cold Therapy Pain Relieving 105 mg/g 79903-0430-03 Walmart 85 g — — FDA listed —
Target Up and Up Pain Relief Menthol Topical Analgesic 10.5 g/100g 82442-0430-03 Target 85 g — — FDA listed —
TIDL PAIN RELIEF CRYO THERAPY original formula Spray. 10.5 g/100mLthis 84214-0001-01 Shenzhen 90 ml — — FDA listed —
TIDL PAIN RELIEF CRYO THERAPY Unscented formula Spray. 10.5 g/100mL 84214-0006-01 Shenzhen 90 ml — — FDA listed —
TIDL Pain Relief CRYO Therapy Limited Edition 10.5 g/100mL 84214-0008-01 Shenzhen 90 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

🏛️
2024
On the market since
Jul 2024
📍
2026
Currently FDA-listed
2 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 3K9958V90M
    A liquid solvent derived from fermentation or chemical synthesis. In medicines, alcohol dissolves active ingredients, helps preserve the product, and improves how the body absorbs certain drugs.
  • 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 BHW853AU9H
    A natural compound found in plants like cloves and hops, beta-caryophyllene is used in medicines as a flavoring agent and to add aroma to the product.
  • 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 XDK00Z8012
    A natural flavoring agent derived from citrus fruits like oranges and lemons. It adds taste and aroma to medicines, making them more pleasant to take, particularly in liquid or chewable formulations.
  • UNII YOW8V9698H
    Dimethyl sulfoxide is a clear liquid solvent derived from wood pulp. In medicines, it helps dissolve or carry active ingredients and improve how the body absorbs the drug.
  • UNII VB06AV5US8
    Echinacea angustifolia is a plant extract used as a natural flavoring or coloring agent in some medicines. It may also help preserve the product's stability or serve as a filler ingredient.
  • UNII W2ZU1RY8B0
    A plant extract from green tea leaves. It's used as an antioxidant ingredient to help preserve the medicine and maintain its stability during storage.
  • UNII 1Q953B4O4F
    Ilex paraguariensis leaf, commonly known as yerba mate, is a plant extract used in medicines as a flavoring agent and to add botanical content. It may also contribute mild preservative properties to the formulation.
  • UNII 0RE8K4LNJS
    Isopropyl myristate is an oily liquid made from coconut or palm oil. It's used in medicines as an emollient and penetration enhancer to help the medicine absorb through skin or improve spreadability in topical products.
  • UNII O84B5194RL
    A plant extract from juniper berries used as a flavoring agent to improve the taste of medicines. It may also contribute mild antimicrobial properties to support product stability.
  • 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 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 Q74T35078H
    Vanilla is a flavoring ingredient extracted from vanilla orchid beans. It's added to medicines to improve taste and make them more pleasant to take, especially for children or patients who need liquid 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.

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

The official label also statesAlcohol Denat, Arnica Montana Flower Extract, Beta-Caryophyllene（Clove）, Calendula Officinalis Flower, Chamomile Extract, Chorus Fruit Extract，Dimethyl Sulfoxide, Echinacea Angustifolia Extract, Green Tea Extract，Ilex Paraguariensis Leaf Extract, Isopropyl Myristate, Juniperus Communis Fruit Extract, Vanilla Extract, Water, White Willow Bark Extract, Oil of Wintergreen.

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

LabelerShenzhen Sam Technology Co., Ltd.
FDA applicationM017 (OTC MONOGRAPH DRUG)
Labeler code84214
First marketedJul 2024
Product typeHuman Otc Drug
Portfolio10 products on file

More NDCs from Shenzhen Sam Technology Co., Ltd. labeler code 84214

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 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 20 words ▾

Use Temporary relief from minor aches and pains of muscles and joints associated with arthritis, simple backache, strains and sprains

⏱️ Dosage and Administration 28 words ▾

Directions ·Adults and children 12 years of age and older：Apply to affected area not more than 3 to 4 times daily ·Children under 12 years of age：Consult physician

⚠️ Warnings 5 words ▾

Warnings For external use only.

🧪 Active Ingredient 4 words ▾

Active Ingredient Menthol 10.5%

🧪 Inactive Ingredients 43 words ▾

Inactive ingredients Alcohol Denat, Arnica Montana Flower Extract, Beta-Caryophyllene（Clove）, Calendula Officinalis Flower, Chamomile Extract, Chorus Fruit Extract，Dimethyl Sulfoxide, Echinacea Angustifolia Extract, Green Tea Extract，Ilex Paraguariensis Leaf Extract, Isopropyl Myristate, Juniperus Communis Fruit Extract, Vanilla Extract, Water, White Willow Bark Extract, Oil of Wintergreen.

🎯 Purpose 3 words ▾

Purpose Topical Anesthetic

📄 Do Not Use 11 words ▾

Do not use While smoking or near heat or open flame

📄 Ask a Doctor Before Use If 24 words ▾

Ask Doctor if condition worsens, or if symptoms persist for more than 7 days, or clear up and reoccur again within a few days

📄 When Using This Product 48 words ▾

When Using ·avoid contact with the eyes or mucous membranes ·do not apply to wounds or damaged skin ·do not apply to irritated skin ·do not bandage ·wash hands after use with cool water ·do not use with heating pad or device ·spray product away from nose,eyes,and mouth

📄 Stop Use and Ask a Doctor If 24 words ▾

Stop Use if condition worsens, or if symptoms persist for more than 7 days, or clear up and reoccur again within a few days

📄 Keep Out of Reach of Children 34 words ▾

Keep Oot Of Reach Of Children If accidentally ingested get medical help or contact a Poison Control Center immediately. Make sure to turn child safety spray lock to off position when not in use.

📄 Questions or Comments 3 words ▾

Questions Call 1(888)778-2986

📄 Package Label / Principal Display Panel 5 words ▾

PRINCIPAL DISPLAY PANEL 1 2

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 Shenzhen Sam Technology Co., Ltd.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Shenzhen Sam Technology 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.
← 84212-0444-50 · AMBIENCE 84214-0002-01 · Shenzhen →
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.