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Vapo Steam 6.2 g/100mL Liquid — NDC 76162-030-08 (Billing 76162-0030-08)

by TOPCO ASSOCIATES, LLC · 1 BOTTLE in 1 CARTON / 240 mL in 1 BOTTLE

This is a package of Vapo Steam 6.2 g/100mL Liquid from TOPCO ASSOCIATES, LLC, marketed since Feb 2023 and currently FDA-listed. It is this product's only package size.

NDC 76162-0030-08
🏷️ FDA NDC (as labeled) 76162-030-08 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

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 76162-030-08
Product NDC 76162-030
11-digit billing NDC 76162003008
RxCUI 701961
UNII 5TJD82A1ET
UPC 0036800501683
Application # M012
SPL Set ID f216f69f-9580-25ac-e053-2995a90a5ac6
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2023-02-01
Route RESPIRATORY (INHALATION)
Dosage form LIQUID
Substance CAMPHOR (SYNTHETIC)
Quick answers
  • RxCUI (RxNorm): 701961
Why two NDCs? The FDA registers this code as 76162-030-08 — 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 → 76162-0030-08. 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?

Vapo Steam is a liquid inhalation product containing synthetic camphor, marketed as an over-the-counter monograph drug. Camphor is a volatile compound that is typically used in inhalation products to produce a cooling or soothing sensation in the respiratory tract. This product is meant to be inhaled as a vapor, commonly used to help with temporary discomfort or congestion during respiratory conditions.

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
76162-0030-08 You're viewing this Main listing 1 BOTTLE in 1 CARTON / 240 mL in 1 BOTTLE 2024-01-11 — 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/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/100mLthis 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

🏛️
2023
On the market since
Feb 2023
📍
2026
Currently FDA-listed
3 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

LabelerTOPCO ASSOCIATES, LLC
FDA applicationM012 (OTC MONOGRAPH DRUG)
Labeler code76162
First marketedFeb 2023
Product typeHuman Otc Drug
Portfolio59 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 📄 Ask a Doctor Before Use If 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 15 words ▾

Uses temporarily relieves cough due to minor throat and bronchial irritation associated with a cold.

⏱️ Dosage and Administration 78 words ▾

Directions see important warnings under "When using this product" adults & children 2 years & over: add 1 tablespoon of solution to each quart of water or 1½ teaspoons of solution to 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 the medicated vapors use up to three times daily or as directed by a doctor children under 2 years: do not use

⚠️ Warnings 160 words ▾

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

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 too close to the face 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 cough lasts more than 7 days, comes back, or occurs with fever, rash, or headache that lasts.

These could be signs of serious condition. Keep out of reach of children. In case of eye exposure (flush eyes with water); or in case of accidental igestion, seek medical help or contact a Poison Control Center right away.

📦 Storage and Handling 13 words ▾

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

🧪 Active Ingredient 5 words ▾

Active ingredient Camphor (Synthetic) 6.2%

🧪 Inactive Ingredients 26 words ▾

Inactive ingredients dimenthicone, eucalyptus globulus (eucalyptus oil) leaf oil, laureth-7, menthol, myristica fragrans (nutmeg) kernel oil, poloxamer 124, SD alcohol 40-B, thuja occidentalis (cedar leaf) oil

🎯 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 52 words ▾

When using this product, do not heat microwave use near an open flame direct steam from the vaporizer too close to the face 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 31 words ▾

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

📄 Keep Out of Reach of Children 32 words ▾

Keep out of reach of children. In case of eye exposure (flush eyes with water); or in case of accidental igestion, seek medical help or contact a Poison Control Center right away.

📄 Package Label / Principal Display Panel 45 words ▾

TopCare® Health Vaporizing Steam Liquid 8 FL OZ (240 mL) - Bottle Label TopCare® Health Vaporizing Steam Liquid 8 FL OZ (240 mL)

TopCare® Health Vaporizing Steam Liquid 8 FL OZ (240 mL) - Carton TopCare® Health Vaporizing Steam Liquid 8 FL OZ (240 mL)

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 — 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 TOPCO ASSOCIATES, LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
TOPCO ASSOCIATES, LLC 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.
← 76162-0029-80 · Topco 76162-0031-56 · TOPCO →
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.