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Air 210 mL/L Gas, 4165 l — NDC 17575-0300-03 package photo

Air 210 mL/L Gas, 4165 l

by AGL Welding Supply Co., Inc. · 4165 L in 1 CYLINDER (17575-300-03)
NDC 17575-0300-03
🏷️ FDA NDC (as labeled) 17575-300-03 billing pads the product segment with a zero
This package
Contains4165 l Pack sizes5 compare ↓
Rx only Brand On market Non-controlled
🗂️ Data synced Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

🆔 Identity & classification

FDA NDC (as labeled) 17575-300-03
Product NDC 17575-300
11-digit billing NDC 17575030003
RxCUI 347856
UNII S88TT14065
Application # NDA205767
SPL Set ID 614223a6-06e2-59b3-e053-2991aa0ac66d
DEA schedule Non-controlled
Marketing category NDA
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 1966-01-01
Route RESPIRATORY (INHALATION)
Dosage form GAS
Substance OXYGEN
Why two NDCs? The FDA registers this code as 17575-300-03 — 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 → 17575-0300-03. 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.

🏭 Manufacturer & labeler

LabelerAGL Welding Supply Co., Inc.
FDA applicationNDA205767 (NDA)
Labeler code17575
First marketedJan 1966
Product typeHuman Prescription Drug
Portfolio2 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.

🩺 Clinical

📗 Our plain-language guide HelloPharmacist
  • ExEm Foam is a contrast agent — think of it like a highlighter for ultrasound. It's made partly from air, which makes it show up as a bright white foam on the ultrasound screen. Yo...
  • What exactly is ExEm Foam, and why does my doctor want to use it?
  • It's common to feel some cramping or pelvic discomfort while the foam is being infused — similar to strong menstrual cramps. Some women also feel a little lightheaded or nauseated...
  • Will I feel anything during the procedure?
📖 Read our full Air guide →
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.

🧪 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.

💲 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: 610 l 3388 l 6570 l 8637 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.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Air 210 mL/L 10297-0103-01 A-OX 680 l FDA listed
Air 210 mL/L 10451-0004-01 General 679 l FDA listed
Air 210 mL/L 11054-0110-01 AIRGAS 105 l Discontinued
Air 210 mL/L 11324-0006-01 Linde 8778 l FDA listed
Air 210 mL/L 11564-0004-04 Fresno 623 l FDA listed
Nitrogen Oxygen Mix 210 mL/L 12213-0733-12 NexAir, 5890 l FDA listed
Air 210 mL/L 14961-0004-01 Haun 606 l FDA listed
Air 210 mL/Lthis 17575-0300-03 AGL 4165 l FDA listed
Compressed Oxygen 21 kg/100L 18087-0007-01 James 170 l FDA listed
Air 210 mL/L 21220-0152-01 General 8778 l FDA listed
Medical Air 210 mL/L 48273-0012-01 Keen 385 l FDA listed
Medical Air 21 L/100L 49221-0025-01 Strate 625 l FDA listed
Air 210 mL/L 50063-0004-01 Andy-Oxy 368 l FDA listed
Air 210 mL/L 51486-0018-01 ILMO 8807 l FDA listed
Air, Compressed 21 L/100L 52374-0006-03 Messer 3000 l FDA listed
Air 210 mL/L 53452-0003-01 Dale 6598 l FDA listed
Air 210 mL/L 55147-0004-03 Minneapolis 3030 l FDA listed
Oxygen 210 mL/L 59400-0001-01 BayCare 670 l Discontinued
Oxygen 210 mg/kg 59400-0005-01 BayCare 34168 kg Discontinued
Air 210 mL/L 64169-0003-01 EUGENE 408 l FDA listed
Reconstituted Air 210 mL/L 68877-0009-01 United 1133 l Discontinued
Air 210 mL/L 70151-0003-01 Central 680 l Discontinued
Air 210 mL/L 72276-0005-01 MITCHELL 190 l FDA listed
Air 210 mL/L 23647-0003-01 SYOXSA, 5974.85 l Discontinued
Air 210 mL/L 43621-0004-01 DJB 6031.5 l FDA listed
Air 210 mL/L 46123-0109-01 Roberts 708 l FDA listed
Air 210 mL/L 67525-0200-01 Spectrum 650 l FDA listed
Air 210 mL/L 49204-0004-01 HARTMAN 420 l FDA listed
About this product: this is the brand-name version. We did not find an FDA-approved generic match for this exact strength, form and route.
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

🏛️
1966
On the market since
Jan 1966
📍
2026
Currently FDA-listed
60 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.

🔬 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 Air — the ingredient across all brands.

Top reported reactions

Cardiac Arrest3
Drug Interaction3
Atrial Fibrillation2
Blood Pressure Decreased2
Cyanosis2
Dystonia2
Oxygen Saturation Decreased2

Age at onset

Adult3

Reporter sex

24 reports
Male · 27%
Female · 73%

Serious outcomes

Hospitalization7
Life-threatening4
Reports over time (by year) — tap or hover for the count & year
2021 2022 2024 2026 3 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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
17575-0300-01 8637 L in 1 CYLINDER (17575-300-01) 1966-01-01 Active
17575-0300-02 6570 L in 1 CYLINDER (17575-300-02) 1966-01-01 Active
17575-0300-03 You're viewing this 4165 L in 1 CYLINDER (17575-300-03) 1966-01-01 Active
17575-0300-04 3388 L in 1 CYLINDER (17575-300-04) 1966-01-01 Active
17575-0300-05 610 L in 1 CYLINDER (17575-300-05) 1966-01-01 Active

You're viewing one of 5 pack sizes for this product.

Pack size FAQ

What quantity is in NDC 17575-0300-03?
NDC 17575-0300-03 contains 4165 l — 4165 l in 1 cylinder.
What is the difference between NDC 17575-0300-03 and NDC 17575-0300-05?
Both are Air 210 mL/L Gas — the drug itself is identical. NDC 17575-0300-03 is the 4165 l package, while NDC 17575-0300-05 is the 610 l package.
What NDC number is used to bill for this package of Air 210 mL/L Gas?
Bill NDC 17575-0300-03 — the 11-digit billing format is 17575030003. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

🧭 About this NDC listing & data coverage

Finished prescription 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) — 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

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 FDA registers it as 17575-300-03, which is what is printed on the packaging and shown on DailyMed. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero: 17575-0300-03, written without dashes as 17575030003. The Identity section at the top of this page lists every form of this code.
What do the three segments of this NDC mean?
In 17575-0300-03, the first segment (17575) is the labeler code FDA assigned to AGL Welding Supply Co., Inc.; the middle segment (0300) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (03) identifies this exact package size and type. Together they name one specific package of one specific product.
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 AGL Welding Supply Co., Inc.. 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 4 other package presentations of this same product, including 610 l (17575-0300-05), 3388 l (17575-0300-04), 6570 l (17575-0300-02). 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?
AGL Welding Supply Co., 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 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.

📄 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.
📄 FDA label 9 words

No readable label sections were found for this product.

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
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.