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Vaporizing Colds Rub Menthol 2.6 g/100g; 1.2 g/100g; 4.73 g/100g Ointment, 113 g — NDC 61734-0030-02 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Vaporizing Colds Rub Menthol 2.6 g/100g; 1.2 g/100g; 4.73 g/100g Ointment, 113 g — NDC 61734-030-02 (Billing 61734-0030-02)

by Delon Laboratories (1990) Ltd · 113 g in 1 JAR

This is a package of 113 g of Vaporizing Colds Rub Menthol 2.6 g/100g; 1.2 g/100g; 4.73 g/100g Ointment from Delon Laboratories (1990) Ltd, marketed since May 2011 and currently FDA-listed. It is the main listing for this product, which comes in 2 package sizes.

NDC 61734-0030-02
🏷️ FDA NDC (as labeled) 61734-030-02 billing pads the product segment with a zero
This package
Contains113 g Pack sizes2 compare ↓
Main listing for product 61734-030 · Also comes in: 50 g 61734-030-03
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 61734-030-02 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
61734 labeler · 030 product · 02 package
Package marketed since
May 24, 2011
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC)
0058342020422
FDA record last changed
Aug 27, 2026
⚠️
Other active recalls for Menthol (different manufacturers) — 1 · tap to view
These affect other manufacturers’ products for the same ingredient — not necessarily the exact NDC on this page.
Class II · Mar 20, 2026 — This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing facility that may bear on product quality. (Xiamen Kang Zhongyuan Biotechnology Co., Ltd.) · FDA recall D-0458-2026
Each entry is an official FDA enforcement report — look up any recall number in the FDA recall database ↗

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 61734-030-02
Product NDC 61734-030
11-digit billing NDC 61734003002
RxCUI 200293
UNII L7T10EIP3A, 2R04ONI662, 5TJD82A1ET
UPC 0058342020422
Application # M012
SPL Set ID 3ed8bc0c-c229-450b-a491-06b578c1b8ee
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2011-05-24
Route TOPICAL
Dosage form OINTMENT
Substance MENTHOL; EUCALYPTUS OIL; CAMPHOR (SYNTHETIC)
Quick answers
  • RxCUI (RxNorm): 200293
Why two NDCs? The FDA registers this code as 61734-030-02 — 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 → 61734-0030-02. 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.

Clinical

📗 Our plain-language guide HelloPharmacist
  • Mostly for temporary relief of minor aches and pains in muscles and joints, like those from arthritis, backache, strains, sprains and bruises. Some products are for other things, s...
  • It depends on the product. Many creams, gels and patches are limited to about 3 to 4 times a day, and patches also have a time limit, often 8 hours. Follow your product label and a...
  • A brief burning feeling can happen when you first apply it and usually fades in several days. But if you get severe burning pain, swelling or blistering, stop using it and call you...
  • No. Don't use menthol products with a heating pad, and avoid local heat or direct sunlight on the area. Rare cases of serious burns have been reported.
📖 Read our full Menthol guide →

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.
Try another pack size: 50 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
61734-0030-02 You're viewing this Main listing 113 g in 1 JAR 2011-05-24 — Active
61734-0030-03 61734-030-03 50 g in 1 JAR 2011-05-24 — Active

You're viewing the largest of 2 pack sizes for this product.

Pack size FAQ

What quantity is in this package?
This package contains 113 g — 113 g in 1 jar.
How does this package differ from NDC 61734-0030-03?
Both are Vaporizing Colds Rub Menthol 2.6 g/100g; 1.2 g/100g; 4.73 g/100g Ointment — the drug itself is identical. This page's package is the 113 g one, while NDC 61734-0030-03 is the 50 g package.
What NDC number is used to bill for this package of Vaporizing Colds Rub Menthol 2.6 g/100g; 1.2 g/100g; 4.73 g/100g Ointment?
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
Walgreens Lavender Chest Rub 47 mg/g; 26 mg/g; 12 mg/g 00363-9802-01 Walgreen 1 jar — — FDA listed —
Mentholatum Cherry Vaporizing Rub 47 mg/g; 12 mg/g; 26 mg/g 10742-8731-01 The 1 jar — — FDA listed —
CVS Health Medicated Chest Rub 47 mg/g; 12 mg/g; 26 mg/g 51316-0200-01 CVS 1 jar — — FDA listed —
VICKS VapoRub .047 g/g; .012 g/g; .026 g/g 58933-0003-01 Procter 1 jar — — FDA listed —
Vicks VapoRub .047 g/g; .012 g/g; .026 g/g 58933-0671-01 Procter 1 jar — — FDA listed —
Vaporizing Colds Rub 2.6 g/100g; 1.2 g/100g; 4.73 g/100gthis 61734-0030-02 Delon 113 g — — FDA listed —
Cough and Cold Therapy For Kids 4.7 g/100g; 2.6 g/100g; 1.2 g/100g 83670-0201-02 Everlaan 1 jar — — 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

🏛️
2011
On the market since
May 2011
📍
2026
Currently FDA-listed
15 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.

What it looks like

Color blue
One label can cover several strengths, so colors may be combined — always confirm a loose pill against the dispensed prescription label or a pharmacist.
Where does this data come from?
Physical description (imprint, shape, color, scoring, coating) from this product’s FDA Structured Product Labeling (SPL), mirrored from DailyMed / openFDA.

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 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 XJ6RUH0O4G
    Turpentine is a volatile liquid derived from pine tree resin. It's used in medicines as a solvent and penetrating agent to help active ingredients dissolve and absorb into the skin or body.

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

The official label also statescedar leaf oil, petrolatum, thymol, turpentine

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

LabelerDelon Laboratories (1990) Ltd
FDA applicationM012 (OTC MONOGRAPH DRUG)
Labeler code61734
First marketedMay 2011
Product typeHuman Otc Drug
Portfolio5 products on file

More NDCs from Delon Laboratories (1990) Ltd labeler code 61734

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 📄 Other Information 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 29 words ▾

Uses temporarily relieves: cough due to minor bronchial irritation associated with a cold or inhaled irritants cough associated with a cold minor aches and pains of muscles and joints

⏱️ Dosage and Administration 71 words ▾

Directions see important warnings under "When using this product" adults and children 2 years and older: rub on the throat and chest in a thick layer cover with a warm, dry cloth if desired clothing should be loose about throat and chest to help vapors reach the nose and mouth use up to three times daily or as directed by a doctor children under 2 years of age: ask a doctor

⚠️ Warnings 158 words ▾

Warnings For external use only; avoid contact with eyes. Do not use: by mouth on wounds or damaged skin in nostrils with tight bandages Ask a doctor before use if you have excessive phlegm (mucus) emphysema persistent or chronic cough asthma cough associated with smoking 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 muscle aches and pains worsen or persist for more than 7 days or clear up and occur again within a few days cough perists for more than 1 week, tends to recur, or is accompanied by fever, rash, or persistent headache. A persistent cough may be a sign of a serious condition. If pregnant 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 9 words ▾

Active ingredients Camphor 4.7% Eucalyptus oil 1.2% Menthol 2.6%

🧪 Inactive Ingredients 8 words ▾

Inactive ingredients cedar leaf oil, petrolatum, thymol, turpentine

🎯 Purpose 13 words ▾

Purpose Cough suppressant & topical analgesic Cough suppressant Cough suppressant & topical analgesic

📄 Do Not Use 15 words ▾

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

📄 Ask a Doctor Before Use If 21 words ▾

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

📄 When Using This Product 25 words ▾

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 59 words ▾

Stop use and ask a doctor if muscle aches and pains worsen or persist for more than 7 days or clear up and occur again within a few days cough perists for more than 1 week, tends to recur, or is accompanied by fever, rash, or persistent headache. A persistent cough may be a sign of a serious condition.

🤰 If Pregnant or Breast-Feeding 10 words ▾

If pregnant 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.

📄 Other Information 6 words ▾

Other information store at room temperature

📄 Package Label / Principal Display Panel 38 words ▾

Penetro1.75oz Penetro Vaporizing Rub 1.75oz Box

Penetro 1.75 oz Label Penetro VCR 1.75 oz Label

Penetro4oz Penetro Vaporizing Medicated Rub 4oz box

Penetro 4oz Label Penetro VCR 4oz Label

PII 4 OZ PII Vaporizing Colds Rub 4 oz

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 Delon Laboratories (1990) Ltd. 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 50 g (61734-0030-03). 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?
Delon Laboratories (1990) 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.
← 61734-0021-03 · Delon 61734-0300-01 · Delon →
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.