Air 210 mL/L Gas, 8070 l
by AIRGAS USA, LLC · 8070 L in 1 CYLINDER (11054-110-41)
NDC 11054-0110-41
🏷️ FDA NDC (as labeled)
11054-110-41
billing pads the product segment with a zero
This package
Contains8070 l
Pack sizes44 compare ↓
Also comes in:
105 l 11054-0110-01
153 l 11054-0110-03
162 l 11054-0110-02
189 l 11054-0110-13
199 l 11054-0110-04
201 l 11054-0110-14
217 l 11054-0110-15
235 l 11054-0110-06
295 l 11054-0110-05
385 l 11054-0110-16
393 l 11054-0110-07
402 l 11054-0110-17
435 l 11054-0110-18
477 l 11054-0110-08
503 l 11054-0110-19
543 l 11054-0110-20
603 l 11054-0110-09
625 l 11054-0110-21
647 l 11054-0110-10
656 l 11054-0110-22
709 l 11054-0110-23
1120 l 11054-0110-24
1210 l 11054-0110-25
1532 l 11054-0110-26
1605 l 11054-0110-11
1655 l 11054-0110-27
2309 l 11054-0110-28
2494 l 11054-0110-29
3109 l 11054-0110-30
3216 l 11054-0110-12
3310 l 11054-0110-31
3795 l 11054-0110-32
4248 l 11054-0110-33
5070 l 11054-0110-34
5654 l 11054-0110-35
6036 l 11054-0110-37
6620 l 11054-0110-38
6760 l 11054-0110-39
6991 l 11054-0110-36
7390 l 11054-0110-40
8800 l 11054-0110-42
10570 l 11054-0110-43
11606 l 11054-0110-44
Rx only
Brand
Discontinued
Non-controlled
⚠ Inactivated by FDA
🗂️ 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 →
⚠️
Excluded from the active FDA NDC Directory.
FDA inactivated this product’s listing record, so it is excluded from the active NDC Directory. The listing was last certified through Dec 2026. A label may still appear on DailyMed, but the NDC is no longer in the current FDA NDC Directory.
Search the FDA NDC Directory ↗
🆔 Identity & classification
FDA NDC (as labeled)
11054-110-41
Product NDC
11054-110
11-digit billing NDC
11054011041
RxCUI
347856
UNII
S88TT14065
Application #
NDA205845
SPL Set ID
ff6d9743-4ec2-4b2c-a19b-ffee5aa81187
DEA schedule
Non-controlled
Marketing category
NDA
Marketing status
Discontinued
FDA listing status
Inactivated by FDA (certified through Dec 2026)
Marketing start
1997-11-06
Route
RESPIRATORY (INHALATION)
Dosage form
GAS
Substance
OXYGEN
Why two NDCs?
The FDA registers this code as 11054-110-41 — 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 → 11054-0110-41. 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
LabelerAIRGAS USA, LLC
FDA applicationNDA205845 (NDA)
Labeler code11054
First marketedNov 1997
Product typeHuman Prescription Drug
Portfolio16 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?
Patient education
Supplement & herbal interactions
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.
💬 Questions about Air?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
🧪 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.
-
790 mL / 1 L
UNII N762921K75
A colorless, odorless gas that makes up most of the air we breathe. In medicines, it's used as a packaging gas or propellant to protect products from oxidation and maintain freshness.
1 inactive ingredient listed in the exact product block matched to this NDC.
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.
💲 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 system | Per each | Per 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:
105 l
153 l
162 l
189 l
199 l
201 l
217 l
235 l
295 l
385 l
393 l
402 l
435 l
477 l
503 l
543 l
603 l
625 l
647 l
656 l
709 l
1120 l
1210 l
1532 l
1605 l
1655 l
2309 l
2494 l
3109 l
3216 l
3310 l
3795 l
4248 l
5070 l
5654 l
6036 l
6620 l
6760 l
6991 l
7390 l
8800 l
10570 l
11606 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
| Product | Labeler | Pack | NADAC/unit | TE | Status | Price 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/Lthis 11054-0110-41 | AIRGAS | 8070 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/L 17575-0300-01 | AGL | 8637 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
🏛️
1997
On the market since
Nov 1997
📍
2026
Currently FDA-listed
29 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
Age at onset
Reporter sex
Male · 27%
Female · 73%
Serious outcomes
Reports over time (by year) — tap or hover for the count & year
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 NDC | Description | Marketing start | Status |
|---|---|---|---|
| 11054-0110-01 | 105 L in 1 CYLINDER (11054-110-01) | 1997-11-06 | Inactivated by FDA |
| 11054-0110-02 | 162 L in 1 CYLINDER (11054-110-02) | 1997-11-06 | Inactivated by FDA |
| 11054-0110-03 | 153 L in 1 CYLINDER (11054-110-03) | 1997-11-06 | Inactivated by FDA |
| 11054-0110-04 | 199 L in 1 CYLINDER (11054-110-04) | 1997-11-06 | Inactivated by FDA |
| 11054-0110-05 | 295 L in 1 CYLINDER (11054-110-05) | 1997-11-06 | Inactivated by FDA |
| 11054-0110-06 | 235 L in 1 CYLINDER (11054-110-06) | 1997-11-06 | Inactivated by FDA |
| 11054-0110-07 | 393 L in 1 CYLINDER (11054-110-07) | 1997-11-06 | Inactivated by FDA |
| 11054-0110-08 | 477 L in 1 CYLINDER (11054-110-08) | 1997-11-06 | Inactivated by FDA |
| 11054-0110-09 | 603 L in 1 CYLINDER (11054-110-09) | 1997-11-06 | Inactivated by FDA |
| 11054-0110-10 | 647 L in 1 CYLINDER (11054-110-10) | 1997-11-06 | Inactivated by FDA |
| 11054-0110-11 | 1605 L in 1 CYLINDER (11054-110-11) | 1997-11-06 | Inactivated by FDA |
| 11054-0110-12 | 3216 L in 1 CYLINDER (11054-110-12) | 1997-11-06 | Inactivated by FDA |
| 11054-0110-13 | 189 L in 1 CYLINDER (11054-110-13) | 1997-11-06 | Inactivated by FDA |
| 11054-0110-14 | 201 L in 1 CYLINDER (11054-110-14) | 1997-11-06 | Inactivated by FDA |
| 11054-0110-15 | 217 L in 1 CYLINDER (11054-110-15) | 1997-11-06 | Inactivated by FDA |
| 11054-0110-16 | 385 L in 1 CYLINDER (11054-110-16) | 1997-11-06 | Inactivated by FDA |
| 11054-0110-17 | 402 L in 1 CYLINDER (11054-110-17) | 1997-11-06 | Inactivated by FDA |
| 11054-0110-18 | 435 L in 1 CYLINDER (11054-110-18) | 1997-11-06 | Inactivated by FDA |
| 11054-0110-19 | 503 L in 1 CYLINDER (11054-110-19) | 1997-11-06 | Inactivated by FDA |
| 11054-0110-20 | 543 L in 1 CYLINDER (11054-110-20) | 1997-11-06 | Inactivated by FDA |
| 11054-0110-21 | 625 L in 1 CYLINDER (11054-110-21) | 1997-11-06 | Inactivated by FDA |
| 11054-0110-22 | 656 L in 1 CYLINDER (11054-110-22) | 1997-11-06 | Inactivated by FDA |
| 11054-0110-23 | 709 L in 1 CYLINDER (11054-110-23) | 1997-11-06 | Inactivated by FDA |
| 11054-0110-24 | 1120 L in 1 CYLINDER (11054-110-24) | 1997-11-06 | Inactivated by FDA |
| 11054-0110-25 | 1210 L in 1 CYLINDER (11054-110-25) | 1997-11-06 | Inactivated by FDA |
| 11054-0110-26 | 1532 L in 1 CYLINDER (11054-110-26) | 1997-11-06 | Inactivated by FDA |
| 11054-0110-27 | 1655 L in 1 CYLINDER (11054-110-27) | 1997-11-06 | Inactivated by FDA |
| 11054-0110-28 | 2309 L in 1 CYLINDER (11054-110-28) | 1997-11-06 | Inactivated by FDA |
| 11054-0110-29 | 2494 L in 1 CYLINDER (11054-110-29) | 1997-11-06 | Inactivated by FDA |
| 11054-0110-30 | 3109 L in 1 CYLINDER (11054-110-30) | 1997-11-06 | Inactivated by FDA |
| 11054-0110-31 | 3310 L in 1 CYLINDER (11054-110-31) | 1997-11-06 | Inactivated by FDA |
| 11054-0110-32 | 3795 L in 1 CYLINDER (11054-110-32) | 1997-11-06 | Inactivated by FDA |
| 11054-0110-33 | 4248 L in 1 CYLINDER (11054-110-33) | 1997-11-06 | Inactivated by FDA |
| 11054-0110-34 | 5070 L in 1 CYLINDER (11054-110-34) | 1997-11-06 | Inactivated by FDA |
| 11054-0110-35 | 5654 L in 1 CYLINDER (11054-110-35) | 1997-11-06 | Inactivated by FDA |
| 11054-0110-36 | 6991 L in 1 CYLINDER (11054-110-36) | 1997-11-06 | Inactivated by FDA |
| 11054-0110-37 | 6036 L in 1 CYLINDER (11054-110-37) | 1997-11-06 | Inactivated by FDA |
| 11054-0110-38 | 6620 L in 1 CYLINDER (11054-110-38) | 1997-11-06 | Inactivated by FDA |
| 11054-0110-39 | 6760 L in 1 CYLINDER (11054-110-39) | 1997-11-06 | Inactivated by FDA |
| 11054-0110-40 | 7390 L in 1 CYLINDER (11054-110-40) | 1997-11-06 | Inactivated by FDA |
| 11054-0110-41 You're viewing this | 8070 L in 1 CYLINDER (11054-110-41) | 1997-11-06 | Inactivated by FDA |
| 11054-0110-42 | 8800 L in 1 CYLINDER (11054-110-42) | 1997-11-06 | Inactivated by FDA |
| 11054-0110-43 | 10570 L in 1 CYLINDER (11054-110-43) | 1997-11-06 | Inactivated by FDA |
| 11054-0110-44 | 11606 L in 1 CYLINDER (11054-110-44) | 1997-11-06 | Inactivated by FDA |
You're viewing one of 44 pack sizes for this product.
Pack size FAQ
What quantity is in NDC 11054-0110-41?
NDC 11054-0110-41 contains 8070 l — 8070 l in 1 cylinder.
What is the difference between NDC 11054-0110-41 and NDC 11054-0110-01?
Both are Air 210 mL/L Gas — the drug itself is identical. NDC 11054-0110-41 is the 8070 l package, while NDC 11054-0110-01 is the 105 l package.
What NDC number is used to bill for this package of Air 210 mL/L Gas?
Bill NDC 11054-0110-41 — the 11-digit billing format is 11054011041. 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
No longer marketed (per FDA listing data)
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
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.
What does the discontinued status mean for this NDC?
The labeler reported a marketing end date (or the listing was delisted), so this specific package is no longer actively marketed. Remaining stock may still be dispensed for a time, and the NDC stays valid for historical records and claims — but data feeds (pricing, labeling) typically stop updating for it. Other package sizes or other manufacturers' versions of the same medication may still be marketed — see the equivalents section where available.
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 11054-110-41, 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: 11054-0110-41, written without dashes as 11054011041. 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 11054-0110-41, the first segment (11054) is the labeler code FDA assigned to AIRGAS USA, LLC; the middle segment (0110) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (41) identifies this exact package size and type. Together they name one specific package of one specific product.
Does this product come in other package sizes?
Yes — the FDA directory lists 43 other package presentations of this same product, including 105 l (11054-0110-01), 153 l (11054-0110-03), 162 l (11054-0110-02). 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?
AIRGAS USA, 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.
📄 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 ▾
No readable label sections were found for this product.
No label section mentions that — try another word, or open the full label on DailyMed below.
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.