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OXYGEN 991 mL/L Gas, 24950 l — NDC 67711-0001-12 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

OXYGEN 991 mL/L Gas, 24950 l — NDC 67711-001-12 (Billing 67711-0001-12)

by AIRSERVE, LLC · 24950 L in 1 DEWAR

This is a package of 24,950 l of OXYGEN 991 mL/L Gas from AIRSERVE, LLC, marketed since Jan 2003 and currently FDA-listed.

NDC 67711-0001-12
🏷️ FDA NDC (as labeled) 67711-001-12 billing pads the product segment with a zero
This package
Contains24950 l Pack sizes19 compare ↓
Product page 67711-0001-01 Also comes in: 40 l 67711-001-10 115 l 67711-001-08 170 l 67711-001-01 170 l 67711-001-07 240 l 67711-001-02 400 l 67711-001-03 682 l 67711-001-04 1723 l 67711-001-09 3455 l 67711-001-06 7108 l 67711-001-05 8881 l 67711-001-19 16750 l 67711-001-13 17780 l 67711-001-18 29069 l 67711-001-15 33500 l 67711-001-11 37619 l 67711-001-14 38300 l 67711-001-17 49200 l 67711-001-16
Rx only 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 67711-001-12 alone.

Record
FDA NDC Directory package listing · Human prescription drug
Code segments
67711 labeler · 001 product · 12 package
Package marketed since
Jan 1, 2003
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 6771100112 3
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 67711-001-12
Product NDC 67711-001
11-digit billing NDC 67711000112
RxCUI 348017
UNII S88TT14065
SPL Set ID f7483c87-439b-4fe2-872e-ebb2b0d5cdbc
DEA schedule Non-controlled
Marketing category UNAPPROVED MEDICAL GAS
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2003-01-01
Route RESPIRATORY (INHALATION)
Dosage form GAS
Substance OXYGEN
Quick answers
  • RxCUI (RxNorm): 348017
Why two NDCs? The FDA registers this code as 67711-001-12 — 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 → 67711-0001-12. 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.

RxNorm drug class

This medicine belongs to the Medical gases class.

Drug family (ATC) Medical gases
Where does this data come from?
Therapeutic classes from RxNorm RxClass (U.S. National Library of Medicine) — Established Pharmacologic Class (FDA), ATC drug family (WHO) and mechanism of action, matched by this product’s RxCUI.

Clinical

📗 Our plain-language guide HelloPharmacist
📖 Read our full Oxygen guide →

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: 40 l 115 l 170 l 170 l 240 l 400 l 682 l 1723 l 3455 l 7108 l 8881 l 16750 l 17780 l 29069 l 33500 l 37619 l 38300 l 49200 l
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
67711-0001-01 67711-001-01 Main listing 170 L in 1 CYLINDER 2003-01-01 — Active
67711-0001-02 67711-001-02 240 L in 1 CYLINDER 2003-01-01 — Active
67711-0001-03 67711-001-03 400 L in 1 CYLINDER 2003-01-01 — Active
67711-0001-04 67711-001-04 682 L in 1 CYLINDER 2003-01-01 — Active
67711-0001-05 67711-001-05 7108 L in 1 CYLINDER 2003-01-01 — Active
67711-0001-06 67711-001-06 3455 L in 1 CYLINDER 2003-01-01 — Active
67711-0001-07 67711-001-07 170 L in 1 CYLINDER 2003-01-01 — Active
67711-0001-08 67711-001-08 115 L in 1 CYLINDER 2003-01-01 — Active
67711-0001-09 67711-001-09 1723 L in 1 CYLINDER 2003-01-01 — Active
67711-0001-10 67711-001-10 40 L in 1 CYLINDER 2003-01-01 — Active
67711-0001-11 67711-001-11 33500 L in 1 DEWAR 2003-01-01 — Active
67711-0001-12 You're viewing this 24950 L in 1 DEWAR 2003-01-01 — Active
67711-0001-13 67711-001-13 16750 L in 1 DEWAR 2003-01-01 — Active
67711-0001-14 67711-001-14 37619 L in 1 DEWAR 2003-01-01 — Active
67711-0001-15 67711-001-15 29069 L in 1 DEWAR 2003-01-01 — Active
67711-0001-16 67711-001-16 49200 L in 1 DEWAR 2003-01-01 — Active
67711-0001-17 67711-001-17 38300 L in 1 DEWAR 2003-01-01 — Active
67711-0001-18 67711-001-18 17780 L in 1 DEWAR 2003-01-01 — Active
67711-0001-19 67711-001-19 8881 L in 1 DEWAR 2003-01-01 — Active

Pack size FAQ

What quantity is in this package?
This package contains 24950 l — 24950 l in 1 dewar.
How does this package differ from NDC 67711-0001-10?
Both are OXYGEN 991 mL/L Gas — the drug itself is identical. This page's package is the 24950 l one, while NDC 67711-0001-10 is the 40 l package.
What NDC number is used to bill for this package of OXYGEN 991 mL/L Gas?
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
Oxygen 991 mL/L 12213-0720-10 NexAir, 9543 l — — FDA listed —
Oxygen 991 mL/L 57924-0001-01 Ross 113 l — — FDA listed —
Oxygen 991 mL/L 66878-0001-01 GC 113 l — — FDA listed —
Oxygen 991 mL/Lthis 67711-0001-12 AIRSERVE, 24950 l — — FDA listed —
Oxygen 991 mL/L 71707-0011-01 TULSA 170 l — — 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

🏛️
2003
On the market since
Jan 2003
📍
2026
Currently FDA-listed
23 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.

A current SPL was checked, but it does not contain a structured or narrative inactive-ingredient list for this product. This does not mean the product has no inactive ingredients.
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

LabelerAIRSERVE, LLC
Labeler code67711
First marketedJan 2003
Product typeHuman Prescription Drug
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.

Full prescribing information FDA SPL

The complete FDA label for this product — the official prescribing information, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
📄 Package Label / Principal Display Panel
📄 Package Label / Principal Display Panel ~2 min read ▾

Gaseous Oxygen Fill Label Warning: For emergency use only when administered by properly trained personnel for oxygen deficiency and resuscitation. For all other medical applications Rx only. Uninterrupted use of high concentration of oxygen over a long duration, without monitoring its effects on oxygen content of arterial blood, may be harmful.

Use only with pressure reducing equipment and apparatus designed for oxygen. Do not attempt to use on patients who have stopped breathing, unless use in conjunction with resuscitative equipment. WARNING: HIGH PRESSURE OXIDIZING GAS.

VIGOROUSLY ACCELERATES COMBUSTION. Keep away from oil, grease and all potential sources of ignition. Open valve slowly and close after each use and when empty.

Store and use with adequate ventilation. Cylinder temperature should not exceed 125F (52C). Use only with equipment cleaned rated for cylinder pressure.

Use a back flow preventative device in the piping. Use this product in accordance with its specific Material Safety Data Sheet CAS 7782-44-7 PRODUCED BY AIR LIQUIFICATION DO NOT REMOVE THIS LABEL AIRSERVE, LLC 26770 LIBERAL CENTER LINE, MI 48015 (586) 427-5349 A 115 LITERS ML6 170 LITERS B 170 LITERS C/F 240 LITERS D 400 LITERS E 682 LITERS M60/Q 1723 LITERS M 3455 LITERS H 7108 LITERS OTHER ___________ LITERS image of gaseous fill label

Liquid Oxygen Fill Label OXYGEN, REFRIGERATED LIQUID USP UN1073 ALWAYS KEEP CONTAINER IN UPRIGHT POSITION WARNING : For emergency use only when administered by properly trained personnel for oxygen deficiency and resuscitation. For all other medical applications, RX only . CAUTION: Federal Law prohibits dispensing without prescription .

Uninterrupted use of high concentrations of oxygen over a long duration, without monitoring its effect on oxygen content of arterial blood, may be harmful. Use only with pressure reducing equipment and apparatus designed for oxygen. Do not attempt to use on patients who have stopped breathing, unless in conjunction with resuscitative equipment.

Produced by Air Liquefaction. WARNING: EXTREMELY COLD OXIDIZING LIQUID AND GAS UNDER PRESSURE. VIGOROUSLY ACCELERATES COMBUSTION.

COMBUSTIBLES IN CONTACT WITH LIQUID OXYGEN MAY EXPLODE ON IGNITION OR IMPACT. CAN CAUSE SEVERE FROSTBITE. Keep oil, grease, and combustibles away. use only equipment cleaned for oxygen service. store and use with adequate ventilation.

Do not get liquid in eyes, wear a face shield and gloves. Do not drop. Use suitable hand truck for container movement.

Avoid spills. Do not walk on or roll equipment over spills. Cylinder temperature should not exceed 52C (125F).

Close valve after each use and when empty. Use in accordance with the Material Safety Data Sheet (MSDS). FIRST AID: IN CASE OF FROSTBITE , obtain medical treatment immediately.

DO NOT REMOVE LABEL AIRSERVE, LLC 26770 LIBERAL AVE, CENTER LINE, MI 48015 (586) 427-5349 image of liquid fill label

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

Finished prescription product Marketed without an FDA application

Listed without an FDA application

This product's marketing category indicates it is marketed without an approved FDA application (no NDA, ANDA, or BLA on file). Having an NDC does not by itself establish FDA approval — the NDC Directory is a listing system, not an approval decision. Approval-linked data such as Orange Book therapeutic-equivalence ratings therefore does not apply.

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) — 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 "Unapproved Medical Gas". 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 AIRSERVE, LLC. 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 18 other package presentations of this same product, including 40 l (67711-0001-10), 115 l (67711-0001-08), 170 l (67711-0001-01). 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?
AIRSERVE, 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 a prescription product, so it is dispensed under a prescriber's order. Your pharmacist can tell you whether any over-the-counter forms of the same medication exist.
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.
← 67706-0031-00 · Macco 67729-0000-25 · PHARMAKINA →
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.