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Assured Vaporizing Chest Rub Camphor and Eucalyptus Oil and Menthol 4.7 g/100g; 1.2 g/100g; 1.25 g/100g Ointment, 113 g — NDC 33992-7991-04 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Assured Vaporizing Chest Rub Camphor and Eucalyptus Oil and Menthol 4.7 g/100g; 1.2 g/100g; 1.25 g/100g Ointment, 113 g — NDC 33992-7991-4 (Billing 33992-7991-04)

by Greenbrier International, Inc. · 113 g in 1 JAR

This is a package of 113 g of Assured Vaporizing Chest Rub Camphor and Eucalyptus Oil and Menthol 4.7 g/100g; 1.2 g/100g; 1.25 g/100g Ointment from Greenbrier International, Inc., marketed since Jun 2018 and currently FDA-listed. It is this product's only package size.

NDC 33992-7991-04
🏷️ FDA NDC (as labeled) 33992-7991-4 billing pads the package 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 33992-7991-4 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
33992 labeler · 7991 product · 4 package
Package marketed since
Jun 26, 2018
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC)
0639277721969
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 33992-7991-4
Product NDC 33992-7991
11-digit billing NDC 33992799104
RxCUI 2003749
UNII 5TJD82A1ET, 2R04ONI662, L7T10EIP3A
UPC 0639277721969
Application # part341
SPL Set ID c7cdbf2f-4841-4a7a-9056-6a741abc3133
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH FINAL
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2018-06-26
Route TOPICAL
Dosage form OINTMENT
Substance CAMPHOR (SYNTHETIC); EUCALYPTUS OIL; MENTHOL
Quick answers
  • RxCUI (RxNorm): 2003749
Why two NDCs? The FDA registers this code as 33992-7991-4 — a 5-4-1 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 package segment → 33992-7991-04. 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?

Assured Vaporizing Chest Rub is an over-the-counter ointment applied to the skin that contains camphor, eucalyptus oil, and menthol. These three ingredients are commonly used together in topical rubs to produce a cooling or warming sensation and are typically included to help ease discomfort associated with minor muscle or joint aches. This product is marketed under FDA's over-the-counter monograph rules for vaporizing rubs.

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 gPer 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
33992-7991-04 You're viewing this Main listing 113 g in 1 JAR 2018-06-26 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Assured Vaporizing Chest Rub 4.7 g/100g; 1.2 g/100g; 1.25 g/100gthis 33992-7991-04 Greenbrier 113 g — — FDA listed —
Assured Vaporizing Chest Rub 4.7 g/100g; 1.2 g/100g; 1.25 g/100g 33992-7992-04 Greenbrier 113 g — — FDA listed —
MedPride Chest Rub .047 g/g; .012 g/g; .0125 g/g 52410-3022-01 Shield 113 g — — FDA listed —
Chest Rub .047 g/g; .012 g/g; .0125 g/g 68747-3022-01 Dabur 113 g — — FDA listed —
Vaporizing chest rub 4.7 g/100g; 1.2 g/100g; 1.25 g/100g 84809-0007-01 LJ 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

🏛️
2018
On the market since
Jun 2018
📍
2026
Currently FDA-listed
8 years 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 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 statesInactive ingredients cedar leaf oil, nutmeg oil, paraffin, petrolatum, thymol, turpentine 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

LabelerGreenbrier International, Inc.
FDA applicationpart341 (OTC MONOGRAPH FINAL)
Labeler code33992
First marketedJun 2018
Product typeHuman Otc Drug
Portfolio5 products on file

More NDCs from Greenbrier International, Inc. labeler code 33992

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 📄 Ask a Doctor Before Use If 📄 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 19 words ▾

Uses Temporarily relieves throat and chest cough nasal congestion due to common cold aching muscles minor aches and pains

⏱️ Dosage and Administration 61 words ▾

Directions see important warnings under "When using this product" children under 2 years of age, ask a doctor before using this product adults and children 2 years and older, rub a thick layer on chest and throat or rub on sore aching muscles. If desired, cover with a dry soft cloth but keep clothing loose. Repeat up to 3 times daily.

⚠️ Warnings 9 words ▾

Warnings For external use only. Avoid contact with eyes.

🧪 Active Ingredient 9 words ▾

Active ingredients Camphor 4.7% Menthol 1.25% Eucalyptus Oil 1.2%

🧪 Inactive Ingredients 12 words ▾

Inactive ingredients cedar leaf oil, nutmeg oil, paraffin, petrolatum, thymol, turpentine oil

🎯 Purpose 9 words ▾

Purpose Cough suppressant/topical analgesic Cough suppressant/topical analgesic Cough suppressant

📄 Do Not Use 15 words ▾

Do not use by mouth in nostrils on wounds or damaged skin with tight bandages

📄 Ask a Doctor Before Use If 21 words ▾

Ask a doctor before use if you have asthama excessive phlegm (mucus) emphysema persistent or chronic cough cough associated with smoking

📄 When Using This Product 29 words ▾

When using this product do not heat microwave use near open flame add to hot water or any container where heating water may cause splattering and result in burns

📄 Stop Use and Ask a Doctor If 42 words ▾

Stop use and ask a doctor if muscle aches/pain persist more than 7 days or come back cough lasts more than 7 days, comes back, or occurs with fever, rash or headache that lasts. These could be signs of a serious conditions.

🤰 If Pregnant or Breast-Feeding 12 words ▾

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

📄 Keep Out of Reach of Children 22 words ▾

Keep out of reach of children. In case of accidental ingestion, get medical help or contact a Poison Control Centre right away.

📄 Package Label / Principal Display Panel 8 words ▾

PRINCIPAL DISPLAY PANEL ASSURED VAPORIZING CHEST RUB 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 Final". 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 Greenbrier International, Inc.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Greenbrier International, Inc. 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.
← 33992-4130-06 · Greenbriar 33992-7992-04 · Greenbrier →
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.