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Vaporizing Chest Rub Lavender 4oz Camphor/Menthol 4.8 g/100g; 1 g/100g Ointment, 113 g — NDC 58503-0171-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Vaporizing Chest Rub Lavender 4oz Camphor/Menthol 4.8 g/100g; 1 g/100g Ointment, 113 g — NDC 58503-171-01 (Billing 58503-0171-01)

by China Ningbo Shangge Cosmetics Technology Corp. · 113 g in 1 JAR

This is a package of 113 g of Vaporizing Chest Rub Lavender 4oz Camphor/Menthol 4.8 g/100g; 1 g/100g Ointment from China Ningbo Shangge Cosmetics Technology Corp., marketed since Feb 2024 and currently FDA-listed. It is this product's only package size.

NDC 58503-0171-01
🏷️ FDA NDC (as labeled) 58503-171-01 billing pads the product segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 8, 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 58503-171-01 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
58503 labeler · 171 product · 01 package
Package marketed since
Feb 1, 2024
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC)
0849607074669
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 58503-171-01
Product NDC 58503-171
11-digit billing NDC 58503017101
RxCUI 2673797
UNII 5TJD82A1ET, L7T10EIP3A
UPC 0849607074669
Application # M012
SPL Set ID 104f5b07-eed2-566c-e063-6294a90a6505
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2024-02-01
Route TOPICAL
Dosage form OINTMENT
Substance CAMPHOR (SYNTHETIC); MENTHOL
Quick answers
  • RxCUI (RxNorm): 2673797
Why two NDCs? The FDA registers this code as 58503-171-01 — 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 → 58503-0171-01. 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?

This is a topical ointment rub marketed as an over-the-counter monograph drug under FDA's standard rules for chest rubs. It contains camphor and menthol as active ingredients, which are commonly used in vaporizing products to create a cooling sensation and the perception of improved breathing comfort when rubbed on the chest and throat. The product is intended for topical use only and is not individually reviewed by the FDA but follows established safety and use guidelines for this category of product.

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
58503-0171-01 You're viewing this Main listing 113 g in 1 JAR 2024-02-01 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Vaporizing Chest Rub Lavender 4oz 4.8 g/100g; 1 g/100g 57337-0160-01 Rejoice 113 g — — FDA listed —
Vapor Stick 1 g/100g; 4.8 g/100g 57337-0180-01 Rejoice 34 g — — FDA listed —
Vaporizing Chest Rub Lavender 4oz 4.8 g/100g; 1 g/100gthis 58503-0171-01 China 113 g — — FDA listed —
Vapor Stick 4.8 g/100g; 1 g/100g 58503-0212-01 China 34 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

🏛️
2024
On the market since
Feb 2024
📍
2026
Currently FDA-listed
2 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 ZBP1YXW0H8
    A fragrant oil extracted from lavender plants, used as a flavoring and scent agent in medicines to improve taste and aroma.
  • 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 statescedar leaf oil;nutmeg oil;petrolatum;fragrance; thymol; turpentine oil; lavender 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

LabelerChina Ningbo Shangge Cosmetics Technology Corp.
FDA applicationM012 (OTC MONOGRAPH DRUG)
Labeler code58503
First marketedFeb 2024
Product typeHuman Otc Drug
Portfolio16 products on file

More NDCs from China Ningbo Shangge Cosmetics Technology Corp. labeler code 58503

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 📄 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 31 words ▾

Uses Use 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 69 words ▾

Directions see important warnings under "When using thi sproduct" adults and children 2 years older: rub a thicj layer on chest & throat or rub on sore aching muscles cover with a warm, dry cloth if desired keep clothing loose about throat/ chest to help vapors reach the nose/mouth repeat up to three times per 24 hours or as directed by doctor children under 2 years: do not use

⚠️ Warnings 178 words ▾

Warnings For external use only; avoid contact with eyes. Do not use Do not use by mouth/in nostrils/ on wounds or damaged skin/ with tight bandages Ask a doctor before use if you have Ask a doctor before use if you have cough that occurs that too much phlegm(mucus) persistent ot chronic cough such as occurs with smoking, asthma or emphysema When using this product 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 Stop use and ask a doctor if muscle aches and pains persist more than 7 days or come back cough lasts more than 7 days, comes back, or occurs with fever, rash, or persistent headache. These could be signs of a serious condition If pregnant or breast-feeding If pregnant or breast-feeding, ask a health professional before use. 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.

📦 Storage and Handling 6 words ▾

Other information store at room temperature

🧪 Active Ingredient 6 words ▾

Active ingredients Camphor 4.8% Menthol 1.0%

🧪 Inactive Ingredients 11 words ▾

Inactive ingredients cedar leaf oil;nutmeg oil;petrolatum;fragrance; thymol; turpentine oil; lavender oil

🎯 Purpose 5 words ▾

Purpose Cough suppressant Topical analgesic

📄 Do Not Use 17 words ▾

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

📄 Ask a Doctor Before Use If 35 words ▾

Ask a doctor before use if you have Ask a doctor before use if you have cough that occurs that too much phlegm(mucus) persistent ot chronic cough such as occurs with smoking, asthma or emphysema

📄 When Using This Product 29 words ▾

When using this product 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 49 words ▾

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

🤰 If Pregnant or Breast-Feeding 14 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 ▾

label label

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 Vaporizing Chest Rub Lavender 4oz (this brand).

Top reported reactions

Asthenia5
Fatigue5
Pneumonia5
Urinary Tract Infection4
Anaemia3
Platelet Count Decreased3
Pruritus3

Age at onset

Adult6
Elderly5

Reporter sex

49 reports
Male · 42%
Female · 58%

Serious outcomes

Hospitalization29
Life-threatening3
Reports over time (by year) — tap or hover for the count & year
2020 2022 2024 2026 7 0
Most recent year is provisional (FAERS lags ~3 months).
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 China Ningbo Shangge Cosmetics Technology Corp.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
China Ningbo Shangge Cosmetics Technology Corp. 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.
← 58503-0170-01 · China 58503-0201-01 · China →
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.