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Rapid Relief Pain Relief Patch Camphor 110mg Menthol 33mg Capsicum Extract 22mg .3 g/100g; .2 g/100g; 1 g/100g Patch, 100 g — NDC 83569-015-01 (Billing 83569-0015-01)

by RAPID AID VIET NAM COMPANY LIMITED · 100 g in 1 POUCH

This is a package of 100 g of Rapid Relief Pain Relief Patch Camphor 110mg Menthol 33mg Capsicum Extract 22mg .3 g/100g; .2 g/100g; 1 g/100g Patch from RAPID AID VIET NAM COMPANY LIMITED, marketed since Nov 2025 and currently FDA-listed. It is the main listing for this product, which comes in 2 package sizes.

NDC 83569-0015-01
🏷️ FDA NDC (as labeled) 83569-015-01 billing pads the product segment with a zero
This package
Contains100 g Pack sizes2 compare ↓
Main listing for product 83569-015 · Also comes in: 500 g 83569-015-05
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Aug 27, 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 83569-015-01 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
83569 labeler · 015 product · 01 package
Package marketed since
Nov 11, 2025
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 8356901501 3
FDA record last changed
Aug 27, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 83569-015-01
Product NDC 83569-015
11-digit billing NDC 83569001501
UNII BZ1R15MTK7, 00UK7646FG, 5TJD82A1ET
Application # M017
SPL Set ID 4360e3be-0ec4-cd57-e063-6394a90aca63
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 2025-11-11
Route TOPICAL
Dosage form PATCH
Substance LEVOMENTHOL; CAPSICUM; CAMPHOR (SYNTHETIC)
Why two NDCs? The FDA registers this code as 83569-015-01 — 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 → 83569-0015-01. 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?

Rapid Relief Pain Relief Patch is a topical patch containing camphor, menthol, and capsicum extract. It is an over-the-counter monograph product marketed under FDA guidelines for its category. The three active ingredients are commonly used together in topical pain relief products to create a warming or cooling sensation on the skin. These substances are typically applied to the skin over areas of minor muscle or joint discomfort, though this listing describes the product composition rather than claiming any specific benefit.

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.
Try another pack size: 500 g
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
83569-0015-01 You're viewing this Main listing 100 g in 1 POUCH 2025-11-11 — Active
83569-0015-05 83569-015-05 1 POUCH in 1 BOX / 500 g in 1 POUCH 2025-11-11 — Active

Pack size FAQ

What quantity is in this package?
This package contains 100 g — 100 g in 1 pouch.
What NDC number is used to bill for this package of Rapid Relief Pain Relief Patch Camphor 110mg Menthol 33mg Capsicum Extract 22mg .3 g/100g; .2 g/100g; 1 g/100g Patch?
Use the 11-digit billing form listed in the identifiers section of this page. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Rapid Relief .3 g/100g; .2 g/100g; 1 g/100gthis 83569-0015-01 RAPID 100 g — — 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
Nov 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.

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

LabelerRAPID AID VIET NAM COMPANY LIMITED
FDA applicationM017 (OTC MONOGRAPH DRUG)
Labeler code83569
First marketedNov 2025
Product typeHuman Otc Drug
Portfolio6 products on file

More NDCs from RAPID AID VIET NAM COMPANY LIMITED labeler code 83569

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 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Ask a Doctor Before Use If 📄 When Using This Product 🤰 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 104 words ▾

Directions Adults and children 12 years of age and older:apply to affected area; change patch 1 to 2 times daily Children under 12 years of age: consult a doctor before use How to Apply: Clean and dry affected area Cut open pouch and remove patch Remove protective film and apply directly to area of pain Apply to affected area not more than 3 times daily. Do not leave on skin for more than a total of 8 hours per day Wash hands with soap after applying patch Reseal pouch containing unused patches Children under 2 years of age: do not use, consult a physician

⚠️ Warnings 5 words ▾

Warnings For external use only.

📦 Storage and Handling 25 words ▾

Other information This product may cause allergic reaction on some individuals • Store in cool dry place away from direct sunlight Store at 15-30°C (59-86°F)

🧪 Active Ingredient 10 words ▾

Active Ingredient(s) Camphor 110mg +Menthol 33mg + Capsicum Extract 22mg

🧪 Inactive Ingredients 22 words ▾

Inactive ingredients Acrylamide/Sodium Acryloyldimethyltaurate Copolymer, Dihydroxyaluminum aminoacetate, DMDM hydantoin, Edetic acid, Glycerin, Laurocapram, Polyacrylic acid, Sodium polyacrylate, Tartaric acid, Titanium dioxide, Water

🎯 Purpose 3 words ▾

Purpose Topical analgesic

📄 Ask a Doctor Before Use If 47 words ▾

Stop use and ask a doctor if: Condition worsens, Severe skin irritation occurs Pain persist for more than 7 days Symptoms clear up and occur again within a few days. You experience pain, swelling or blistering, as rare but serious burns can occur headache or redness occurs

📄 When Using This Product 70 words ▾

When using this product: Use only as directed do not get into eyes or on mucous membranes. If contact occurs, rinse thoroughly with water do not apply to wounds, damaged or irritated skin do not bandage or cover with any type of wrap except clothing do not use with a heating pad or apply external heat do not use 1 hour prior to bathing or within 30 minutes after bathing

🤰 If Pregnant or Breast-Feeding 16 words ▾

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

📄 Keep Out of Reach of Children 25 words ▾

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

📄 Package Label / Principal Display Panel 2 words ▾

IAMGE IMAGE

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 — 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 RAPID AID VIET NAM COMPANY LIMITED. Listing status can change — the directory data on this page refreshes weekly.
Does this product come in other package sizes?
Yes — the FDA directory lists 1 other package presentation of this same product, including 1 pouch (83569-0015-05). Each has its own NDC and its own page — see the package list near the top of this page.
Who lists this product with the FDA?
RAPID AID VIET NAM COMPANY LIMITED 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.
← 83569-0014-01 · RAPID 83569-0016-06 · RAPID →
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.