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Vapor Stick Camphor/Menthol 1 g/100g; 4.8 g/100g Stick, 40 g — NDC 57337-0180-02 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Vapor Stick Camphor/Menthol 1 g/100g; 4.8 g/100g Stick, 40 g — NDC 57337-180-02 (Billing 57337-0180-02)

by Rejoice International Corp. · 40 g in 1 BOTTLE

This is a package of 40 g of Vapor Stick Camphor/Menthol 1 g/100g; 4.8 g/100g Stick from Rejoice International Corp., marketed since Apr 2025 and currently FDA-listed.

NDC 57337-0180-02
🏷️ FDA NDC (as labeled) 57337-180-02 billing pads the product segment with a zero
This package
Contains40 g Pack sizes2 compare ↓
Product page 57337-0180-01 Also comes in: 34 g 57337-180-01
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

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 57337-180-02
Product NDC 57337-180
11-digit billing NDC 57337018002
RxCUI 2673797
UNII L7T10EIP3A, N20HL7Q941
Application # M012
SPL Set ID 33d1fbf3-d33c-58b9-e063-6294a90ae098
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2025-04-28
Route TOPICAL
Dosage form STICK
Substance MENTHOL; CAMPHOR (NATURAL)
Quick answers
  • RxCUI (RxNorm): 2673797
Why two NDCs? The FDA registers this code as 57337-180-02 — 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 → 57337-0180-02. 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

🧪 What is this product?

This is a topical stick product containing camphor and menthol, marketed as an over-the-counter monograph drug. Camphor and menthol are commonly used in vapor rubs and topical products for their cooling and warming sensations on the skin. These ingredients are typically used to provide temporary relief of minor aches and to create a soothing effect in products applied directly to the body.

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.
Try another pack size: 34 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
57337-0180-01 57337-180-01 Main listing 34 g in 1 BOTTLE 2025-04-28 — Active
57337-0180-02 You're viewing this 40 g in 1 BOTTLE 2025-10-13 — 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 40 g — 40 g in 1 bottle.
How does this package differ from NDC 57337-0180-01?
Both are Vapor Stick Camphor/Menthol 1 g/100g; 4.8 g/100g Stick — the drug itself is identical. This page's package is the 40 g one, while NDC 57337-0180-01 is the 34 g package.
What NDC number is used to bill for this package of Vapor Stick Camphor/Menthol 1 g/100g; 4.8 g/100g Stick?
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
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/100gthis 57337-0180-02 Rejoice 40 g — — FDA listed —
Vaporizing Chest Rub Lavender 4oz 4.8 g/100g; 1 g/100g 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

🏛️
2025
On the market since
Apr 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.

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 PDC6A3C0OX
    Glycerin is a clear, thick liquid derived from plant oils or fats. It acts as a humectant to retain moisture, a sweetener, and a solvent in medications.
  • 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 HIE492ZZ3T
    Phenoxyethanol is a synthetic preservative and antimicrobial agent used to prevent bacterial and fungal growth in medicines and cosmetic products, extending shelf life and maintaining product safety.
  • UNII 451W47IQ8X
    Sodium chloride is common table salt. It's used in medicines as a buffer to maintain proper pH, as a filler to add bulk, or to adjust the osmotic balance in liquid formulations.
  • UNII JQ43KP6296
    Sodium palmitate is a salt derived from palmitic acid, a naturally occurring fatty acid. It acts as an emulsifier and surfactant in medicines, helping mix oil and water-based ingredients and improving product stability and texture.
  • UNII 059QF0KO0R
    Water is a liquid solvent that dissolves and mixes ingredients together in liquid medicines, syrups, and injections. It helps distribute the active drug evenly throughout the product.
  • UNII TTV12P4NEE
    Xanthan gum is a thickening and stabilizing ingredient made from fermented corn or other sugars. It's added to medicines to improve texture, prevent separation of liquids and solids, and help the product stay consistent.

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

The official label also statesWater Sodium Palmitate Petrolatum Glycerin Sodium Chloride Fragrance Phenoxyethanol Xanthan Gum

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

LabelerRejoice International Corp.
FDA applicationM012 (OTC MONOGRAPH DRUG)
Labeler code57337
First marketedApr 2025
Product typeHuman Otc Drug
Portfolio62 products on file
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 32 words ▾

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

⏱️ Dosage and Administration 71 words ▾

Directions see important warnings under :When using this product adult and children 2 years and older: rub a thick 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 167 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 with too much phlegm (mucus); persistent or chronic cough such as occurs with smoking, asthma or emphysema 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 Stop use and ask a doctor if muscle asches and pains persist more than days or come back; cough lasts more than 7 days, come back, or occurs with fever, rash, or persistent headache. These could be signs 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.

📦 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 13 words ▾

Inactive ingredients Water Sodium Palmitate Petrolatum Glycerin Sodium Chloride Fragrance Phenoxyethanol Xanthan Gum

🎯 Purpose 5 words ▾

Purpose Cough suppressant Topical analgesic

📄 Do Not Use 18 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 36 words ▾

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

📄 When Using This Product 26 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 49 words ▾

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

📄 Package Label / Principal Display Panel 3 words ▾

label 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 Vapor Stick (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
Disabling1
Reports over time (by year) — tap or hover for the count & year
2020 2022 2024 2026 7 3
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 Rejoice International Corp.. 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 34 g (57337-0180-01). 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?
Rejoice International 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.
← 57337-0179-01 · Rejoice 57337-0181-01 · Rejoice →
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.