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Vicks Vaposteam Lavender CAMPHOR, (-)- .062 g/mL Inhalant — NDC 69901-0523-08 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Vicks Vaposteam Lavender CAMPHOR, (-)- .062 g/mL Inhalant — NDC 69901-523-08 (Billing 69901-0523-08)

by Kaz USA, Inc · 1 BOTTLE, PLASTIC in 1 BOX / 236 mL in 1 BOTTLE, PLASTIC

This is a package of Vicks Vaposteam Lavender CAMPHOR, (-)- .062 g/mL Inhalant from Kaz USA, Inc, marketed since Jan 2025 and currently FDA-listed. It is this product's only package size.

NDC 69901-0523-08
🏷️ FDA NDC (as labeled) 69901-523-08 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

NDC database record

One package, one record: these facts belong to NDC 69901-523-08 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
69901 labeler · 523 product · 08 package
Package marketed since
Jan 5, 2025
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 6990152308 8
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 69901-523-08
Product NDC 69901-523
11-digit billing NDC 69901052308
RxCUI 701961
UNII 213N3S8275
Application # M012
SPL Set ID 03bf6b78-cf8e-44c6-bae0-5bd0a85f8aa9
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2025-01-05
Route RESPIRATORY (INHALATION)
Dosage form INHALANT
Substance CAMPHOR, (-)-
Quick answers
  • RxCUI (RxNorm): 701961
Why two NDCs? The FDA registers this code as 69901-523-08 — 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 → 69901-0523-08. 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?

Vicks Vaposteam Lavender is an over-the-counter inhalant product containing camphor. This monograph drug is designed to be inhaled through the respiratory tract, typically from a warm vapor mist. Camphor is commonly used in inhalant products to help open airways and provide a cooling or soothing sensation during inhalation. This type of product is marketed under FDA rules for over-the-counter inhalant drugs.

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.
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
69901-0523-08 You're viewing this Main listing 1 BOTTLE, PLASTIC in 1 BOX / 236 mL in 1 BOTTLE, PLASTIC 2025-01-05 — 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/mL 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/mLthis 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

🏛️
2025
On the market since
Jan 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 3K9958V90M
    A liquid solvent derived from fermentation or chemical synthesis. In medicines, alcohol dissolves active ingredients, helps preserve the product, and improves how the body absorbs certain drugs.
  • 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 92RU3N3Y1O
    Dimethicone is a silicone-based oil that acts as an anti-foaming agent and lubricant in medicines. It reduces gas bubbles in liquid formulations and helps coat and protect the stomach lining when ingested.
  • UNII 2R04ONI662
    Eucalyptus oil is a fragrant liquid extracted from eucalyptus tree leaves. It's used in medicines as a flavor, scent, or soothing agent in topical products and cough preparations.
  • UNII Z95S6G8201
    A synthetic surfactant derived from lauryl alcohol and ethylene oxide. It helps dissolve and mix oily and watery ingredients in liquid formulations, and may improve how the medicine spreads or is absorbed.
  • UNII ZBP1YXW0H8
    A fragrant oil extracted from lavender plants, used as a flavoring and scent agent in medicines to improve taste and aroma.
  • UNII L7T10EIP3A
    A cooling compound from mint plants used as a flavoring agent and to create a fresh sensation in medicines. It helps mask bitter tastes and improve how the product feels in the mouth.
  • 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 1S66E28KXA
    Poloxamer 124 is a synthetic polymer that acts as a surfactant and solubilizer in medicines. It helps dissolve and stabilize active ingredients, particularly in liquid formulations and gels.

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

The official label also statesAlcohol, Cedar Leaf Oil, Silicone, Eucalyptus Oil, Laureth-7, Lavender Oil, Menthol, Nutmeg Oil, Poloxamer 124

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

LabelerKaz USA, Inc
FDA applicationM012 (OTC MONOGRAPH DRUG)
Labeler code69901
First marketedJan 2025
Product typeHuman Otc Drug
Portfolio2 products on file

More NDCs from Kaz USA, Inc labeler code 69901

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 📄 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 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 45 words ▾

Uses temporarily relieves cough associated with a cold temporarily helps you cough less. cough suppressant which temporarily controls the impulse to cough. temporarily helps to suppress the cough reflex that causes coughing. temporarily reduces the intensity of coughing. reduces your cough to help you rest.

⏱️ Dosage and Administration 104 words ▾

Directions see important warnings under " When using this product ". adults & children 2 years & over: add 1 tablespoonful of solution to each quart of water OR 1½ teaspoonfuls of solution to each pint of water OR add 0.5 fl oz (1 tablespoonful) of VapoSteam liquid to medicine cup found on Warm Mist and Cool Mist Humidifiers that accept VapoSteam. follow manufacturer's directions for using vaporizer. add solution directly to cold water only in a hot steam vaporizer. breathe in the medicated vapors. use up to three times daily or as directed by a doctor. children under 2 years: do not use.

⚠️ Warnings 179 words ▾

Warnings For external use only. Flammable Keep away from fire or flame. For steam inhalation only.

DO NOT TAKE BY MOUTH. Ask a doctor before use if you have a persistent or chronic cough such as occurs with smoking, asthma or emphysema. cough that occurs with too much phlegm (mucus). When using this product, do not heat microwave use near an open flame direct steam from the vaporizer or humidifier too close to the face. add to hot water or any container where heating water except when adding to cold water in a hot steam vaporizer.

May cause splattering and result in burns. Stop use and ask a doctor if cough persists 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. In case of eye exposure flush eyes with water; or if swallowed, get medical help or contact a Poison Control Center right away.

📦 Storage and Handling 22 words ▾

Other information close container tightly and store at room temperature 68°-77° F (20°-25° C) and away from direct sunlight. contains 78% alcohol

🧪 Active Ingredient 5 words ▾

Active ingredient Camphor (Synthetic) 6.2%

🧪 Inactive Ingredients 17 words ▾

Inactive ingredients Alcohol, Cedar Leaf Oil, Silicone, Eucalyptus Oil, Laureth-7, Lavender Oil, Menthol, Nutmeg Oil, Poloxamer 124

🎯 Purpose 3 words ▾

Purpose Cough suppressant

📄 Ask a Doctor Before Use If 29 words ▾

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

📄 When Using This Product 53 words ▾

When using this product, do not heat microwave use near an open flame direct steam from the vaporizer or humidifier too close to the face. add to hot water or any container where heating water except when adding to cold water 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 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 29 words ▾

Keep out of reach of children. In case of eye exposure flush eyes with water; or if swallowed, get medical help or contact a Poison Control Center right away.

📄 Questions or Comments 10 words ▾

Questions? 1-800-VAPOR-1-2 (1-800-827-6712) Monday – Friday 8am to 6pm EST.

📄 Package Label / Principal Display Panel 40 words ▾

PRINCIPAL DISPLAY PANEL - 236 ml Bottle Box VICKS Vapo Steam Lavender COUGH SUPPRESSANT Produces Calming Medicated Vapors to Help Relieve Coughs 8 FL OZ (236 ml) DO NOT TAKE BY MOUTH PRINCIPAL DISPLAY PANEL - 236 ml Bottle Box

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 CAMPHOR, (-)- — the ingredient across all brands.

Top reported reactions

Pain228
Fatigue210
Headache170
Nausea167
Dyspnoea165
Diarrhoea151
Cough131

Age at onset

Neonate1
Infant3
Child10
Adolescent6
Adult214
Elderly186

Reporter sex

3,223 reports
Male · 31%
Female · 68%
Unknown · 0%

Serious outcomes

Hospitalization742
Death162
Disabling118
Life-threatening78
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 359 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 Kaz USA, Inc. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Kaz USA, 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.
← 69901-0522-08 · Kaz 69903-0001-30 · Shinpharma →
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.