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Bonica EaseX Pain Relieving CAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATE 31 mg/g; 60 mg/g; 100 mg/g Patch, 360 patches — NDC 75568-0036-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Bonica EaseX Pain Relieving CAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATE 31 mg/g; 60 mg/g; 100 mg/g Patch, 360 patches — NDC 75568-036-01 (Billing 75568-0036-01)

by Planet (Anhui) Pharmaceutical Co., Ltd. · 1 POUCH in 1 BOX / 360 PATCH in 1 POUCH / .33 g in 1 PATCH

This is a package of 360 patches of Bonica EaseX Pain Relieving CAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATE 31 mg/g; 60 mg/g; 100 mg/g Patch from Planet (Anhui) Pharmaceutical Co., Ltd., marketed since Jul 2025 and currently FDA-listed. It is this product's only package size.

NDC 75568-0036-01
🏷️ FDA NDC (as labeled) 75568-036-01 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 75568-036-01 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
75568 labeler · 036 product · 01 package
Package marketed since
Jul 1, 2025
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 7556803601 4
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 75568-036-01
Product NDC 75568-036
11-digit billing NDC 75568003601
RxCUI 1793147
UNII 5TJD82A1ET, L7T10EIP3A, LAV5U5022Y
Application # M
SPL Set ID 34f1196a-fda1-4bef-be71-e5a09ee97bc1
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2025-07-01
Route TOPICAL
Dosage form PATCH
Substance CAMPHOR (SYNTHETIC); MENTHOL; METHYL SALICYLATE
Quick answers
  • RxCUI (RxNorm): 1793147
Why two NDCs? The FDA registers this code as 75568-036-01 — 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 → 75568-0036-01. 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

🧪 What is this product?

Bonica EaseX Pain Relieving is a topical patch containing camphor, menthol, and methyl salicylate. This product is an over-the-counter monograph drug, meaning it follows FDA's established rules for its category rather than being individually reviewed. The three active ingredients are typically used as counterirritants, which means they create a warming or cooling sensation on the skin to help temporarily ease minor muscle and joint discomfort when applied directly to 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.

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
75568-0036-01 You're viewing this Main listing 1 POUCH in 1 BOX / 360 PATCH in 1 POUCH / .33 g in 1 PATCH 2025-07-01 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Large Medicate Relief Patches 3.1 g/100g; 6 g/100g; 10 g/100g 46122-0645-13 Amerisource 6 patches $0.665 — Availability likely —
Pain Relief Patches 3.1 g/100g; 6 g/100g; 10 g/100g 70000-0368-01 Cardinal 6 patches $0.665 — Availability likely —
Pain Relief Patches 3.1 g/100g; 6 g/100g; 10 g/100g 00363-0907-60 Walgreen 60 patches — — FDA listed —
Walgreens Pain Relieving Patch 100 mg/g; 31 mg/g; 60 mg/g 00363-6716-06 Walgreen 6 patches — — FDA listed —
Large Pain Relieving 3.1 g/100g; 6 g/100g; 10 g/100g 00363-9904-06 Walgreen 6 pouches — — FDA listed —
Pain Relief Medicated 3.1 g/100g; 6 g/100g; 10 g/100g 11822-7883-03 RITE 60 pouches — — FDA listed —
Medicated Pain Relief Patch 3.1 g/100g; 6 g/100g; 10 g/100g 30142-0892-60 Kroger 60 patches — — FDA listed —
Topcare Medicated Pain Relieving Patch 60ct 60 mg/g; 31 mg/g; 100 mg/g 36800-0750-60 Topco 1 pouch — — FDA listed —
Large Medicated Pain Relief Patches 3.1 g/100g; 6 g/100g; 10 g/100g 41250-0833-05 Meijer 6 patches — — FDA listed —
Medicated Pain Relief Patches 3.1 g/100g; 6 g/100g; 10 g/100g 41250-0907-60 Meijer 60 patches — — FDA listed —
Pain Relief Patches 3.1 g/100g; 6 g/100g; 10 g/100g 46122-0392-58 Amerisource 40 patches — — Discontinued —
Salonpas 21.56 mg/1; 41.73 mg/1; 69.55 mg 46581-0110-14 Hisamitsu 140 patches — — FDA listed —
Salonpas 86.24 mg/1; 166.92 mg/1; 278.2 mg 46581-0210-06 Hisamitsu 6 patches — — FDA listed —
Pain-Relieving Patch 60 mg/g; 100 mg/g; 31 mg/g 51316-0280-60 CVS 180 patches — — FDA listed —
CVS Health Pain-Relieving Patch 10 g/100g; 3.1 g/100g; 6 g/100g 51316-0992-06 CVS 6 patches — — FDA listed —
Medicated Pain Relief Patches 3.1 g/100g; 6 g/100g; 10 g/100g 53943-0907-60 Discount 60 patches — — FDA listed —
Solstice Pain Relieving 3.1 g/100g; 6 g/100g; 10 g/100g 55614-0210-02 MADISON 2 patches — — FDA listed —
Solstice Pain Relieving 3.1 g/100g; 6 g/100g; 10 g/100g 55614-0310-06 MADISON 6 patches — — FDA listed —
Dollar General Medicated Pain Relief Patch 3.1 g/100g; 6 g/100g; 10 g/100g 55910-0907-20 DOLGENCORP, 20 patches — — FDA listed —
HealthWise 3x Medicated Pain Relief Patch 120 Bulk 10 g/1; 3.1 g/1; 6 g 71101-0032-12 Veridian 120 patches — — FDA listed —
HealthWise 3x Medicated Pain Relief Patch 10 g/1; 3.1 g/1; 6 g 71101-0034-01 Veridian 18 patches — — FDA listed —
TheraCare Medicated Pain Relief 6 g/100g; 3.1 g/100g; 10 g/100g 71101-0128-01 Veridian 60 patches — — FDA listed —
TheraCare Medicated Pain Relief Patches 3.1 g/100g; 6 g/100g; 10 g/100g 71101-0909-06 Veridian 6 patches — — FDA listed —
AsperFlex Advance 86.24 mg/1; 166.92 mg/1; 278.2 mg 71399-4458-06 Akron 6 patches — — FDA listed —
Pain Relief Patches 3.1 g/100g; 6 g/100g; 10 g/100g 72036-0907-60 Harris 60 patches — — FDA listed —
Bonica EaseX Pain Relieving 31 mg/g; 60 mg/g; 100 mg/gthis 75568-0036-01 Planet 360 patches — — FDA listed —
Careland Pain Relief Plus 31 mg/g; 60 mg/g; 100 mg/g 75568-0039-01 Planet 56 pouches — — FDA listed —
Careland Kinesiology Pain Relieving Tape 31 mg/g; 60 mg/g; 100 mg/g 75568-0049-00 Planet 20 patches — — FDA listed —
Equate Pain Relief Patch Camphor/Menthol/Salicylate 3.1 g/100g; 6 g/100g; 10 g/100g 79903-0039-60 Walmart 60 pouches — — FDA listed —
Equate Medicated Pain Relieving Patch, Large 6-Count 3.1 g/100g; 6 g/100g; 10 g/100g 79903-0308-06 Walmart 6 pouches — — FDA listed —
Sc Herbal .06 g/g; .1 g/g; .031 g/g 82198-0015-01 Big 3 patches — — FDA listed —
Pain Relief Patch 3.1 g/1; 6 g/1; 10 g 83324-0255-60 CDMA, 60 patches — — FDA listed —
Pain 10 g/1001; 3.1 g/1001; 6 g/1001 87255-0005-01 Shenzhen 1 patch — — 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

🏛️
2025
On the market since
Jul 2025
📍
2026
Currently FDA-listed
1 year 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.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • UNII T5L8T28FGP
    Mineral oil is a clear, odorless liquid derived from crude oil. It acts as a lubricant and emollient in medications, helping pills slide smoothly during manufacturing and aiding moisture retention in topical products.
  • UNII 255PIF62MS
    A synthetic antioxidant compound used to prevent oils and fats in medications from breaking down or becoming rancid during storage. It helps maintain the medicine's stability and shelf life.
  • UNII GR35AH6YDN
    A sticky plant-derived resin containing terpenes, natural compounds from trees and plants. Used as a binder and adhesive in some tablet and capsule formulations to help hold ingredients together.

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

The official label also states• A-tocopherol acetate • Antioxidant 1010 • ESIS • Fumed Silica • Mineral Oil • Polyisobutylene • Terpene Resin

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

LabelerPlanet (Anhui) Pharmaceutical Co., Ltd.
FDA applicationM (OTC MONOGRAPH DRUG)
Labeler code75568
First marketedJul 2025
Product typeHuman Otc Drug
Portfolio21 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 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 6 words ▾

Use For temporary relief of pain

⏱️ Dosage and Administration 72 words ▾

Directions Adults and children 12 years of age and over: • Clean and dry affected area • Carefully remove backing from patch • Apply sticky side of patch to affected area • Use one patch for up to 8 hours • Discard patch after single use • Apply 1 patch at a time to affected area, not more than 3 to 4 times daily Children under 12 years of age:consult a physician

⚠️ Warnings ~1 min read ▾

Warnings For external use only Do not use • More than one patch on your body at a time • On cut, irritated or swollen skin • On puncture wounds • For more than one week without consulting a doctor • If you are allergic to any active or inactive ingredients • If pouch is damaged or opened When using this product • Use only as directed • Read and follow all directions and warnings • Do not allow contact with the eyes • Do not use at the same time as other topical anesthetics • Do not bandage tightly or apply local heat (such as heating pads) to the area of use • Do not microwave • Dispose of used patch in manner that always keeps product away from children and pets.

Used patches still contain the drug product that can product serious adverse effects is a child or pet chews or ingests this patch. Stop use and ask a doctor if • Conditions worsen • Redness is present • Irritation develops • Symptoms persist for more than 7 days or clear up and occur again within a few days • You experience signs of skin injury, such as pain, swelling, or blistering where the product was applied If pregant 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 12 words ▾

Active ingredients Camphor 3.1% Menthol 6.0% Methyl salicylate 10.0% Purpose Topical analgesic

🧪 Inactive Ingredients 21 words ▾

Inactive ingredients • A-tocopherol acetate • Antioxidant 1010 • ESIS • Fumed Silica • Mineral Oil • Polyisobutylene • Terpene Resin

🎯 Purpose 3 words ▾

Purpose Topical analgesic

📄 Do Not Use 53 words ▾

Do not use • More than one patch on your body at a time • On cut, irritated or swollen skin • On puncture wounds • For more than one week without consulting a doctor • If you are allergic to any active or inactive ingredients • If pouch is damaged or opened

📄 When Using This Product 98 words ▾

When using this product • Use only as directed • Read and follow all directions and warnings • Do not allow contact with the eyes • Do not use at the same time as other topical anesthetics • Do not bandage tightly or apply local heat (such as heating pads) to the area of use • Do not microwave • Dispose of used patch in manner that always keeps product away from children and pets. Used patches still contain the drug product that can product serious adverse effects is a child or pet chews or ingests this patch.

📄 Stop Use and Ask a Doctor If 53 words ▾

Stop use and ask a doctor if • Conditions worsen • Redness is present • Irritation develops • Symptoms persist for more than 7 days or clear up and occur again within a few days • You experience signs of skin injury, such as pain, swelling, or blistering where the product was applied

🤰 If Pregnant or Breast-Feeding 11 words ▾

If pregant 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.

📄 Package Label / Principal Display Panel 3 words ▾

Package Labeling: Label

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 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.
← 75568-0035-01 · Planet 75568-0037-01 · 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.