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Doue Vaporizing Chest Rub Cough Suppressant Camphor, Menthol, Eucalyptus Oil 4.7 g/100g; 1 g/100g; 1 g/100g Jelly, 113 g — NDC 87510-0005-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Doue Vaporizing Chest Rub Cough Suppressant Camphor, Menthol, Eucalyptus Oil 4.7 g/100g; 1 g/100g; 1 g/100g Jelly, 113 g — NDC 87510-005-01 (Billing 87510-0005-01)

by ONEST LIMITED · 113 g in 1 JAR

This is a package of 113 g of Doue Vaporizing Chest Rub Cough Suppressant Camphor, Menthol, Eucalyptus Oil 4.7 g/100g; 1 g/100g; 1 g/100g Jelly from ONEST LIMITED, marketed since Apr 2026 and currently FDA-listed. It is this product's only package size.

NDC 87510-0005-01
🏷️ FDA NDC (as labeled) 87510-005-01 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 Sep 17, 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 87510-005-01 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
87510 labeler · 005 product · 01 package
Package marketed since
Apr 25, 2026
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC)
0604052318801
FDA record last changed
Sep 17, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 87510-005-01
Product NDC 87510-005
11-digit billing NDC 87510000501
RxCUI 1042788
UNII N20HL7Q941, L7T10EIP3A, 2R04ONI662
UPC 0604052318801
Application # M012
SPL Set ID 2089c28b-98fd-4797-8940-b0749d8b5df7
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-04-25
Route TOPICAL
Dosage form JELLY
Substance CAMPHOR (NATURAL); MENTHOL; EUCALYPTUS OIL
Quick answers
  • RxCUI (RxNorm): 1042788
Why two NDCs? The FDA registers this code as 87510-005-01 — 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 → 87510-0005-01. 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?

Doue Vaporizing Chest Rub is a topical jelly marketed as an over-the-counter cough suppressant. It contains camphor, menthol, and eucalyptus oil, three aromatic ingredients commonly used in vapor rub products for topical application to the chest and throat. These ingredients are typically included to produce a cooling or warming sensation and strong aroma, with the intention of providing comfort during cough or congestion. This product is marketed under FDA's over-the-counter monograph rules for this drug category.

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
87510-0005-01 You're viewing this Main listing 113 g in 1 JAR 2026-04-25 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Chestrub 4.7 g/100g; 1 g/100g; 1 g/100g 20276-0100-31 Delta 113 g — — FDA listed —
Med Aid Chest Rub 1 g/100g; 4.7 g/100g; 1 g/100g 22431-0123-01 Blue 113 g — — FDA listed —
Assured Vaporizing Chest Rub 4.7 g/100g; 1 g/100g; 1 g/100g 33992-7996-04 Greenbrier 113 g — — FDA listed —
Doue Vaporizing Chest Rub Cough Suppressant 4.7 g/100g; 1 g/100g; 1 g/100gthis 87510-0005-01 ONEST 113 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

🏛️
2026
On the market since
Apr 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.

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

  • UNII BJ169U4NLG
    Cedar leaf oil is a fragrant extract from cedar tree foliage used as a flavoring agent and fragrance in medications to improve taste and aroma, making the medicine more pleasant to take.
  • 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 Z1CLM48948
    Nutmeg oil is a natural aromatic extract from nutmeg seeds. It's used in medicines as a flavoring agent to improve taste and sometimes as a fragrance to mask bitter or unpleasant odors.
  • UNII 4T6H12BN9U
    Petrolatum is a purified mineral oil-based jelly derived from petroleum. In medicines, it acts as an emollient, lubricant, and moisture barrier to soften skin, reduce friction, and help prevent water loss from formulations.
  • UNII 3J50XA376E
    Thymol is a natural compound derived from thyme and other plants. It acts as a preservative and flavoring agent in medicines, helping prevent microbial growth and add taste.
  • UNII C5H0QJ6V7F
    Turpentine oil is a volatile liquid extracted from pine tree resin. It's used in some formulations as a solvent and flavoring agent to help dissolve other ingredients and add taste.

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

The official label also statesPetrolatum, Mineral Oil, Nutmeg Oil, Turpentine Oil, Thymol, Cedar Leaf Oil

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

LabelerONEST LIMITED
FDA applicationM012 (OTC MONOGRAPH DRUG)
Labeler code87510
First marketedApr 2026
Product typeHuman Otc Drug
Portfolio6 products on file

More NDCs from ONEST LIMITED labeler code 87510

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 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 32 words ▾

Uses • On chest and throat, helps temporarily relieve cough as may occur with common cold and minor bronchial irritation. • For the temporary relief of pain associated with minor skin irritation.

⏱️ Dosage and Administration 65 words ▾

Direction • See important warning under “when using this product “. Adults and children 2 years and over: • Rub a thick layer on the chest and throat • keep clothing loose around the chest/ throat to help vapors reach the nose/ mouth. • use up to 3 times daily or as directed by a doctor. Children under 2 years of age: ask a doctor.

⚠️ Warnings 126 words ▾

Warning For external use only. Avoid contact with the eyes. Do not take by mouth or place in nostrils.

Do not use • By mouth • in nostrils • With tight bandages • On wound-damaged skin • With persistent on chronic cough such as occurs with asthma, emphysema or smoking. Ask the doctor if you have , • Cough that occurs with too much phlegm (Mucus). When using this product, do not heat microwave Add to hot water or any container where heating water, may cause splattering and result in burns.

Stop use and ask a doctor if : • cough that lasts more than 7 days, comes back, or occurs with fever, rash, or persistent headache. • These could be signs of a serious condition.

🧪 Active Ingredient 16 words ▾

Active Ingredient Purpose Camphor ............4.7% ...................... Cough Suppressant Menthol..............1.0% ...................... Topical Analgesic Eucalyptus Oil......1.0%...................... Nasal Decongestion

🧪 Inactive Ingredients 13 words ▾

Inactive ingredients Petrolatum, Mineral Oil, Nutmeg Oil, Turpentine Oil, Thymol, Cedar Leaf Oil

📄 Package Label / Principal Display Panel 4 words ▾

Product label image description

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 Camphor, Menthol, Eucalyptus Oil — the ingredient across all brands.

Top reported reactions

Eye Colour Change1

Reporter sex

1 reports
Female · 100%
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 ✓ 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 ONEST LIMITED. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
ONEST 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.
← 87510-0004-01 · ONEST 87510-0006-01 · ONEST →
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.