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Yeheal Camphor, Menthol, Isopropyl Alcohol 2 mg/100mg; 2 mg/100mg; 75 mg/100mg Spray — NDC 87008-0813-02 package photo

Yeheal Camphor, Menthol, Isopropyl Alcohol 2 mg/100mg; 2 mg/100mg; 75 mg/100mg Spray

by Shenzhen Yeheal Biotechnology Co., Ltd · 1 BOTTLE, SPRAY in 1 BOX (87008-813-02) / 90 mg in 1 BOTTLE, SPRAY (87008-813-01)
NDC 87008-0813-02
🏷️ FDA NDC (as labeled) 87008-813-02 billing pads the product segment with a zero
OTC On market Non-controlled
🗂️ Data synced 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

🆔 Identity & classification

FDA NDC (as labeled) 87008-813-02
Product NDC 87008-813
11-digit billing NDC 87008081302
UNII 213N3S8275, L7T10EIP3A, ND2M416302
Application # M017
SPL Set ID 3cf1bc74-3060-6d63-e063-6294a90a9f5c
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2025-08-13
Route TOPICAL
Dosage form SPRAY
Substance CAMPHOR, (-)-; MENTHOL; ISOPROPYL ALCOHOL
Why two NDCs? The FDA registers this code as 87008-813-02 — 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 → 87008-0813-02. 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

LabelerShenzhen Yeheal Biotechnology Co., Ltd
FDA applicationM017 (OTC MONOGRAPH DRUG)
Labeler code87008
First marketedAug 2025
Product typeHuman Otc Drug
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

🧪 What is this product?

Yeheal is a topical spray containing camphor, menthol, and isopropyl alcohol. This is an over-the-counter monograph product, meaning it is marketed under FDA rules for its drug category rather than as an individually reviewed application. Camphor and menthol are typically used in topical products for their cooling and warming sensations on the skin, and are commonly found in products intended to provide temporary relief. Isopropyl alcohol functions as a solvent and antiseptic ingredient in the spray formulation.

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.

🧪 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 IM7ZCU30YH
    A plant material derived from Dictamnus dasycarpus, used in traditional formulations. It may function as a natural ingredient or botanical extract to support product stability or therapeutic properties.
  • UNII 06T1X86LXT
    A plant-derived ingredient from Gentiana scabra (Asian gentian), used as a natural flavoring and bitter agent to enhance taste or mask unpleasant flavors in medicines.
  • UNII O3E12ZLW5T
    A plant extract from houttuynia cordata, an herb used in traditional Asian medicine. It may serve as a natural flavoring agent or botanical additive in the formulation.
  • UNII VYT2JA85NH
    A plant extract from cogon grass roots used in some formulations. It may serve as a natural filler, thickening agent, or ingredient to help bind tablet components together.
  • UNII 2Q2191ZXBC
    A plant material derived from Oldenlandia herbacea, an herb traditionally used in some formulations. It may serve as a natural ingredient or filler in the product.
  • UNII CCO8AM4KTX
    A plant extract derived from the whole Persicaria perfoliata plant, also known as mile-a-minute weed. It may serve as a natural flavoring agent, colorant, or botanical filler in the formulation.
  • UNII Y45L13XZ2U
    Prunella vulgaris is a plant extract used in some medications as a flavoring agent or traditional ingredient. It may help mask bitter tastes or contribute mild flavor to the formulation.
  • UNII 49G13A93VE
    A plant extract from the bark of the golden larch tree, used in herbal or botanical formulations for its traditional properties. It may serve as an active botanical ingredient or natural additive in certain supplement or traditional medicine products.
  • UNII 1VDG5Y5HS6
    A plant extract from Japanese knotweed used as a natural colorant and antioxidant in medications. It helps preserve the medicine and may provide a reddish or purple tint to tablets or capsules.
  • UNII 701QX6SO4L
    A plant extract from the roots of madder, traditionally used in herbal medicine. It may function as a natural colorant or flavoring agent in some formulations.
  • UNII X8KX602M5L
    Sophora flavescens is a plant extract used in medicines as a natural thickening agent and skin-conditioning ingredient. It helps adjust the medicine's texture and may support formulation stability.
  • UNII 77J6094Z2H
    A plant-derived substance from the root of Sophora tonkinensis. Used in traditional formulations as a natural binder and to support product consistency and stability.

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

The official label also statesSophora tonkinensis, Pseudolaric Bark,Cogongrass RhizomeLobelia chinensis, Reynoutria japonica, Persicaria perfoliata,Gentiana scabra, Houttuynia cordata, Rubia cordifolia, Prunellavulgaris, Hedyotis diffusa, Sophora flavescens, Dittany Bark.

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.

💲 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.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Yeheal 2 mg/100mg; 2 mg/100mg; 75 mg/100mgthis 87008-0813-02 Shenzhen 1 bottle — — 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
Aug 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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
87008-0813-02 You're viewing this 1 BOTTLE, SPRAY in 1 BOX (87008-813-02) / 90 mg in 1 BOTTLE, SPRAY (87008-813-01) 2025-08-13 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) ✓ 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 87008-813-02, 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: 87008-0813-02, written without dashes as 87008081302. 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 87008-0813-02, the first segment (87008) is the labeler code FDA assigned to Shenzhen Yeheal Biotechnology Co., Ltd; the middle segment (0813) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (02) 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 Shenzhen Yeheal Biotechnology Co., Ltd. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Shenzhen Yeheal Biotechnology 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 17 words ▾

Temporarily relieves itching and discomfort from insect bites orminor skin irritations ,Provides mild antibacterial effect for skin

⏱️ Dosage and Administration 24 words ▾

Adults and children 2 years and older: Apply 3 to 4 times daily to the affected area. Children under 2 years: Ask a doctor.

⚠️ Warnings 44 words ▾

For external use only Flammable: Keep away from heat or flameAvoid contact with eyes . Stop use and ask a doctor if rash, irritationor symptoms worsen Keep out of reach of children. lf swallowedget medical help or contact a Poison Control Center right away

🧪 Active Ingredient 7 words ▾

Camphor(2%)-----External analgesic Menthol(2%)---External analgesic Isopropyl Alcohol(75%)----------- Antiseptic

🧪 Inactive Ingredients 22 words ▾

Sophora tonkinensis, Pseudolaric Bark,Cogongrass RhizomeLobelia chinensis, Reynoutria japonica, Persicaria perfoliata,Gentiana scabra, Houttuynia cordata, Rubia cordifolia, Prunellavulgaris, Hedyotis diffusa, Sophora flavescens, Dittany Bark.

🎯 Purpose 3 words ▾

External analgesic Antiseptic

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 87007-0001-01 · Shandong 87009-0001-01 · Saptagir →
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.