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BonicaEaseX Hot Capsicum Pain Relieving .25 mg Patch, 24 patches — NDC 75568-042-00 (Billing 75568-0042-00)

by Planet (Anhui) Pharmaceutical Co.,Ltd · 8 POUCH in 1 BOX / 3 PATCH in 1 POUCH / 2.8 PATCH in 1 PATCH

This is a package of 24 patches of BonicaEaseX Hot Capsicum Pain Relieving .25 mg Patch from Planet (Anhui) Pharmaceutical Co.,Ltd, marketed since Mar 2026 and currently FDA-listed. It is this product's only package size.

NDC 75568-0042-00
🏷️ FDA NDC (as labeled) 75568-042-00 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

NDC database record

One package, one record: these facts belong to NDC 75568-042-00 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
75568 labeler · 042 product · 00 package
Package marketed since
Mar 15, 2026
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC-A, from the NDC)
3 7556804200 8
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 75568-042-00
Product NDC 75568-042
11-digit billing NDC 75568004200
RxCUI 1043399
UNII 00UK7646FG
Application # M017
SPL Set ID ca6e48af-af6d-4808-a576-0319d2080d38
Established class (EPC) Non-Standardized Plant Allergenic Extract; Non-Standardized Food Allergenic Extract
Physiologic effect Increased Histamine Release; Cell-mediated Immunity
Chemical class Allergens; Dietary Proteins; Plant Proteins; Vegetable Proteins
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-03-15
Route TOPICAL
Dosage form PATCH
Substance CAPSICUM
Quick answers
  • RxCUI (RxNorm): 1043399
Why two NDCs? The FDA registers this code as 75568-042-00 — 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 → 75568-0042-00. 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.

RxNorm drug class

This medicine belongs to the Capsaicin and similar agents class.

Drug family (ATC) Capsaicin and similar agents, Other local anesthetics
Where does this data come from?
Therapeutic classes from RxNorm RxClass (U.S. National Library of Medicine) — Established Pharmacologic Class (FDA), ATC drug family (WHO) and mechanism of action, matched by this product’s RxCUI.

Clinical

📗 Our plain-language guide HelloPharmacist
  • It gives temporary relief of minor aches and pains in muscles and joints. That includes pain from simple backache, arthritis, strains, bruises and sprains.
  • Clean and dry the area, then put the patch on intact skin right after taking it out of the pouch. Adults can use up to 3 patches a day, one at a time, and each should come off with...
  • You may notice a burning feeling, and warm water, sweat or heat can make it stronger. Avoid use within an hour before or after a shower, bath, sauna or hard exercise. Never use it...
  • Keep it off your face, eyes, other mucous membranes, and any wounds or irritated, broken, sunburned or chapped skin. If it gets in your eyes, rinse continually with cool water and...
📖 Read our full Capsaicin Topical 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 eachPer 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
75568-0042-00 You're viewing this Main listing 8 POUCH in 1 BOX / 3 PATCH in 1 POUCH / 2.8 PATCH in 1 PATCH 2026-03-15 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Good Neighbor Capsaicin Heat Patch for Back .025 g/100g 46122-0753-55 Amerisource 3 patches $1.117 — Availability likely —
Capsaicin Hot Patches .025 g/100g 70000-0556-01 Cardinal 2 patches $1.117 — Availability likely —
Capsimide .025 g/100g 70512-0016-10 Sola 10 pouches $1.117 — Availability likely —
Walgreens Capsaicin Hot Patch .25 mg/g 00363-6691-03 Walgreen 3 patches — — FDA listed —
Capsaicin Heat Patches Back And Large Areas .025 g/100g 00363-9902-03 Walgreen 3 patches — — FDA listed —
WellPatch Warming Pain Relief 25 mg 10742-8127-01 The 1 patch — — FDA listed —
Capsaicin Heat Patches Pain Relief .025 g/100g 11822-4210-03 Rite 3 patches — — FDA listed —
Capsaicin Heat Patches Back And Large Areas .025 g/100g 41250-0842-03 Meijer 3 patches — — FDA listed —
Salonpas-Hot Capsicum .025 g/100g 46581-0700-01 Hisamitsu 1 patch — — Discontinued —
Equate Capsaicin Pain Relieving .25 mg/g 49035-0890-01 Wal-Mart 1 patch — — FDA listed —
Satogesic Hot .25 mg 49873-0608-01 Sato 5 patches — — FDA listed —
Capsaicin .025 g/100g 50488-2025-01 Alexso, 10 patches — — FDA listed —
Capsaicin Heat .025 g/100g 52000-0040-41 Universal 2 patches — — FDA listed —
Solstice Capsaicin Patch Hot .025 g/100g 55614-0410-01 MADISON 1 patch — — FDA listed —
CVS Medicated Heat 1 ct .025 g/g 59779-0770-01 CVS 1 g — — FDA listed —
Best Choice Targeted Warming Capsaicin Heat Patch .025 g/100g 63941-0691-03 Valu 3 patches — — FDA listed —
Coralite Medicated Heat 249 mg 65923-0123-01 United 1 patch — — FDA listed —
Coralite Capsaicin Heat Patch 2ct 249 mg/g 65923-0809-02 United 1 patch — — FDA listed —
Capsaicin Pain Relief .702 mg 67510-0303-01 Kareway 1 patch — — FDA listed —
Capsaicin .025 g/100g 69420-7025-01 SA3, 10 patches — — FDA listed —
Capsaicin .025 g/100g 71436-3025-01 ARI 10 patches — — FDA listed —
Pain Relieving Gel-Patch .00025 g/g 73557-0180-05 Shanghai 5 patches — — FDA listed —
BonicaEaseX Hot Capsicum Pain Relieving .25 mgthis 75568-0042-00 Planet 24 patches — — FDA listed —
Meijer Capsaicin Heat Patch .025 g/100g 79481-0064-03 Meijer 3 patches — — FDA listed —
Capsaicin .025 g/100g 79643-0002-01 PHARMACURE 10 patches — — FDA listed —
Capsaicin 0.025% 2.5 mg/10g 80425-0541-01 Advanced 30 patches — — FDA listed —
CAPSAICIN HEAT Patch .025 g/1001 83559-0013-01 Henan 48 patches — — FDA listed —
Rapid Relief .00025 g/g 83569-0018-06 RAPID 6 patches — — FDA listed —
Honest Med Capsaicin Patch .025 g/100g 84097-0003-24 Proper 24 patches — — FDA listed —
Capsaicin 0.025% 2.5 mg/10g 85096-0401-30 Marcella 30 patches — — FDA listed —
0.025% Capsaicin Pain relief Patch .025 g/100g 85323-0001-00 Xuzhou 5 patches — — FDA listed —
0.025% Capsaicin Pain relief Patch .025 g/100g 85323-0005-01 Xuzhou 48 patches — — 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.

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 Capsaicin Topical 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.

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

LabelerPlanet (Anhui) Pharmaceutical Co.,Ltd
FDA applicationM017 (OTC MONOGRAPH DRUG)
Labeler code75568
First marketedMar 2026
Product typeHuman Otc Drug
Portfolio3 products on file

More NDCs from Planet (Anhui) Pharmaceutical Co.,Ltd labeler code 75568

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 📄 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 26 words ▾

Uses For temporary relief of minor aches & pains of muscles & joints associated with: • simple backache • arthritis • strains • bruises • sprains

⏱️ Dosage and Administration 39 words ▾

Directions Adults and children 12 years of age and over: • clean and dry affected area • remove patch from film • Use one patch for up to 24 hours Children under 12 years of age: consult a doctor

⚠️ Warnings 144 words ▾

Warnings For external use only Do not use • on wounds or damaged skin- with a heating pad • if you are allergic to any ingredients of this product When using this product • use only as directed • avoid contact with the eyes, mucous membranes or rashes • do not bandage tightly • discontinue use at least 1 hour before a bath or shower• do not use immediately after a bath or shower Stop use and ask a doctor if skin reactions such as redness, itching, rash, excessive irritation, burning sensation, swelling or blistering occur conditions worsen- symptoms persist for more than 7 days symptoms clear up and occur again within a few days If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

🧪 Active Ingredient 10 words ▾

Active ingredient Capsicum extract 0.025% as Capsaicin Purpose Topical analgesic

🧪 Inactive Ingredients 30 words ▾

Inactive ingredients • Propylene Glycol • Titanium Dioxide • Isopropyl Myristate • Polyisobutylene • Vitamin E Acetate • Mineral Oil • Dimethyl Isosorbide • Tri(2,4-Ditertrabutylphenyl)phosphiteester • 3,5-Di-tert-butyl-4-hydroxyhydrocinnamic acid neopentanetetrayl ester

🎯 Purpose 3 words ▾

Purpose Topical analgesic

📄 Do Not Use 24 words ▾

Do not use • on wounds or damaged skin- with a heating pad • if you are allergic to any ingredients of this product

📄 When Using This Product 45 words ▾

When using this product • use only as directed • avoid contact with the eyes, mucous membranes or rashes • do not bandage tightly • discontinue use at least 1 hour before a bath or shower• do not use immediately after a bath or shower

📄 Stop Use and Ask a Doctor If 41 words ▾

Stop use and ask a doctor if skin reactions such as redness, itching, rash, excessive irritation, burning sensation, swelling or blistering occur conditions worsen- symptoms persist for more than 7 days symptoms clear up and occur again within a few 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, get medical help or contact a Poison Control Center right away.

📄 Questions or Comments 6 words ▾

Questions or comments? 1-816-716-0852 Monday-Friday 9AM-5PM

📄 Package Label / Principal Display Panel 3 words ▾

Package Labeling: Label02

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 BonicaEaseX Hot Capsicum Pain Relieving (this brand).

Top reported reactions

Immune Thrombocytopenia7
Weight Increased7
Diarrhoea3
Dyspnoea3
Nasopharyngitis3
Amnesia2
Anaemia2

Reporter sex

0 reports

Serious outcomes

Hospitalization7
Life-threatening4
Disabling3
Death1
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 4 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 Planet (Anhui) Pharmaceutical Co.,Ltd. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Planet (Anhui) Pharmaceutical 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.
← 75568-0041-00 · Planet 75568-0043-00 · Planet →
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.