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Vaporizing Camphor 62 mg/mL Liquid, 237 mL — NDC 41250-024-34 (Billing 41250-0024-34)

by Meijer, Inc. · 237 mL in 1 BOTTLE, PLASTIC

This is a package of 237 mL of Vaporizing Camphor 62 mg/mL Liquid from Meijer, Inc., marketed since Jul 2011 and currently FDA-listed. It is this product's only package size.

NDC 41250-0024-34
🏷️ FDA NDC (as labeled) 41250-024-34 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 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

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 41250-024-34
Product NDC 41250-024
11-digit billing NDC 41250002434
RxCUI 701961
UNII N20HL7Q941
UPC 0713733369305
Application # M012
SPL Set ID 7afc98d7-f64f-42d5-9022-28ad6b01db8a
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2011-07-22
Route RESPIRATORY (INHALATION)
Dosage form LIQUID
Substance CAMPHOR (NATURAL)
Quick answers
  • RxCUI (RxNorm): 701961
Why two NDCs? The FDA registers this code as 41250-024-34 — 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 → 41250-0024-34. 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 an over-the-counter inhalable liquid containing natural camphor. The product is intended to be vaporized and inhaled, a delivery method commonly used for aromatic respiratory products. Camphor is typically used in such products for its cooling and soothing sensations in the nasal passages and airways. This product is marketed under FDA's monograph rules for OTC inhalable products in this 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 mLPer 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
41250-0024-34 You're viewing this Main listing 237 mL in 1 BOTTLE, PLASTIC 2011-07-22 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
GNP Vapor Steam camphor (synthetic) .062 g/mL 46122-0762-29 AmerisourceBergen 1 bottle $0.019 — Availability likely —
Leader Vapor Steam camphor (synthetic) .062 g/mL 70000-0563-01 LEADER/Cardinal 1 bottle $0.019 — Availability likely —
Vaporizing 62 mg/mL 00363-0055-34 Walgreen 1 bottle — — FDA listed —
Weeks and Leo Medicated Vaporizing Steam .623 g/10mL 11383-0256-04 Weeks 1 bottle — — FDA listed —
Rite Aid Pharmacy congestion relief vaporizing steam 6.2 g/100mL 11822-3506-08 Rite 1 bottle — — FDA listed —
Vaporizing Steam Liquid 62 mg/mL 13709-0332-01 NeilMed 1 bottle — — FDA listed —
Vaproizing 62 mg/mL 37808-0397-34 H 1 bottle — — FDA listed —
Vaporizing 62 mg/mLthis 41250-0024-34 Meijer, 237 ml — — FDA listed —
Discount Drug Mart Value Vapor Steam .623 g/10mL 53943-0256-08 Drug 1 bottle — — FDA listed —
Dollar General Vapor Steam .623 g/10mL 55910-0256-08 DOLGENCORP, 1 bottle — — FDA listed —
Best Choice Vapor Steam .623 g/10mL 63941-0256-04 Valu 1 bottle — — FDA listed —
CVS Vapor Steam .623 g/10mL 69842-0256-04 CVS 1 bottle — — Discontinued —
Vicks VapoSteam .062 g/mL 69901-0522-08 Kaz 1 bottle — — FDA listed —
Vicks Vaposteam Lavender .062 g/mL 69901-0523-08 Kaz 1 bottle — — FDA listed —
Vaporizing 62 mg/mL 72288-0397-34 Amazon.com 1 bottle — — FDA listed —
Vapo Steam 6.2 g/100mL 76162-0030-08 TOPCO 1 bottle — — FDA listed —
Quality Choice Vapor Steam .623 g/10mL 83324-0266-04 Chain 1 bottle — — 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
Jul 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.

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.

Loading inactive ingredients from the official FDA label in the background. No external source is being called by this page request.
Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.

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

LabelerMeijer, Inc.
FDA applicationM012 (OTC MONOGRAPH DRUG)
Labeler code41250
First marketedJul 2011
Product typeHuman Otc Drug
Portfolio202 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 and Cautions ⚠️ Warnings 🤒 Adverse Reactions 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Ask a Doctor Before Use If 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Other Information 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 8 words ▾

Use temporarily relieves cough associated with a cold

⏱️ Dosage and Administration 75 words ▾

Directions see important warnings under "When using this product" adults and children 2 years and older: use 1 tablespoon of solution for each quart of water or 1 1/2 teaspoons of solution for each pint of water add solution directly to cold water only in a hot steam vaporizer follow manufacturer's directions for using vaporizer breathe in medicated vapors may be repeated up to 3 times a day children uner 2 years: ask a doctor

⚠️ Warnings and Cautions 7 words ▾

Flammable keep away from fire or flame

⚠️ Warnings 14 words ▾

Warnings For External use only For steam inhalation only. Do not take by mouth.

🤒 Adverse Reactions 12 words ▾

Adverse Reactoions DIST. BY MEIJER DISTRIBUTION, INC. GRAND RAPIDS, MI 49544 www.meijer.com

📦 Storage and Handling 13 words ▾

Other information close container tightly and store at room temperature away from heat

🧪 Active Ingredient 4 words ▾

Active ingredient Camphor 6.2%

🧪 Inactive Ingredients 25 words ▾

Inactive ingredients alcohol 82%, dimethicone, Eucalyptus globulus leaf oil, laureth-7, menthol, Myristica fragrans (nutmeg) kernel oil, poloxamer 124, Thuja occidentalis leaf oil (cedar leaf oil)

🎯 Purpose 3 words ▾

Purpose Cough suppressant

📄 Ask a Doctor Before Use If 25 words ▾

Ask a doctor a persistent or chronic cough such as occurs with smoking, emphysema or asthma a cough that occurs with too much phlegm (mucus)

📄 When Using This Product 41 words ▾

When using this product do not heat microwave use near open flame add to hot water or any container where heating water except when adding to cold water only in a hot steam vaporizer. May cause splattering and result in burns.

📄 Stop Use and Ask a Doctor If 37 words ▾

Stop use and ask a doctor if cough persists for more than 1 week, tends to recur or is accompanied by fever, rash or persistant headache. A persistant cough may be a sign of a serious condition.

📄 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 23 words ▾

Warnings Failure to follow these warnings could result in serious consequences. Do not use if printed seal under cap is broken or missing.

📄 Questions or Comments 2 words ▾

Questions? 1-888-593-0593

📄 Package Label / Principal Display Panel 46 words ▾

Principal display panel NDC 41250-024-34 meijer ® MEDICATED Vaporizing Steam Liquid COMPARE TO VICKS ® VAPO STEAM ® ACTIVE INGREDIENTS* COUGH SUPPRESSANT Relieves cough to help you rest Liquid medication for hot steam vaporizers CAUTION: NOT FOR INTERNAL USE 8 FL OZ (237 mL) 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 Vaporizing (this brand).

Top reported reactions

Fatigue30
Drug Hypersensitivity29
Pain29
Pruritus26
Headache24
Pneumonia24
Dyspnoea23

Age at onset

Neonate1
Infant1
Adolescent1
Adult19
Elderly16

Reporter sex

167 reports
Male · 39%
Female · 61%

Serious outcomes

Hospitalization76
Life-threatening9
Reports over time (by year) — tap or hover for the count & year
2020 2022 2024 2026 32 2
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 — Not published for this NDC No photo available yet for this listing.
Inactive ingredients (structured) — Not published for this NDC The labeler did not submit a structured excipient list, or no SPL is 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 Meijer, Inc.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Meijer, 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.
← 41250-0007-30 · Meijer, 41250-0029-29 · Meijer →
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.