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Prescription medicine

Air

Official FDA data, not advice

Everything here comes from the U.S. Food and Drug Administration (FDA): the drug label, the NDC Directory, Drugs@FDA, recall reports and the drug shortage list. Each fact shows its source and date.

This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or change any medicine.

In an emergency, call 911. If someone may have taken too much of a medicine, call Poison Help: 1‑800‑222‑1222.

Quick answers

Does Air have a boxed warning?
No. None of the 9 FDA labels we found for this medicine has a boxed warning.
Is there a shortage of Air?
No current shortage is listed by the FDA for the products of this medicine (FDA data from October 30, 2026).
Has Air been recalled?
FDA enforcement reports list 2 recalls of products of this medicine; the newest started September 16, 2015 (Class III). A recall usually concerns specific lots, not every product.
Who makes Air?
14 companies list prescription products of Air in the FDA NDC Directory, including Linde Gas & Equipment Inc., NexAir, LLC and Cee-Kay Supply, Inc..

What Air is used for

We did not find an “Indications and Usage” section in the FDA labels for this medicine. See the label on DailyMed →

This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or change any medicine.

Boxed warning

A boxed warning (“black box”) is the FDA’s strongest warning on a drug label, for serious or life-threatening risks.

The label quoted above has no boxed warning.

0 of 9 FDA labels for this medicine have a boxed warning.

Forms and how it is given

Dosage formsGas
RouteRespiratory (inhalation)
Prescription products14 in the FDA NDC Directory

Companies that list this medicine

Labelers in the FDA NDC Directory: the company named on the package (maker or distributor), with the number of prescription products.

FDA approval history

  • NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
Brand and biologic applications
ApplicationSponsorApprovedLater changes approved
NDA205796
MEDICAL AIR, USP
Machine & Welding Supply CoJuly 13, 2013 —
NDA205804
MEDICAL AIR, USP
Purity Cylinder Gases, IncJuly 14, 2013 —
NDA205821
MEDICAL AIR, USP
Scott-Gross CompanyJuly 14, 2013 —
NDA205826
MEDICAL AIR, USP
Dupuy OxygenJuly 15, 2013 —
NDA205847
MEDICAL AIR, USP
Oxarc IncJuly 20, 2013 —
NDA205859
MEDICAL AIR, USP
NexairJuly 23, 2013 —
NDA205890
MEDICAL AIR, USP
Matheson Tri-Gas IncAugust 2, 2013 —
NDA205909
MEDICAL AIR, USP
Praxair Distribution IncAugust 5, 2013 —
NDA205910
MEDICAL AIR, USP
Praxair Distribution Mid-Atlantic LLCAugust 5, 2013 —
NDA207036
MEDICAL AIR, USP
Cee Kay SupplyApril 22, 2014 —

Shortage status

The FDA drug shortage list does not show these products.

FDA Drug Shortages database →

Recalls

From FDA enforcement reports, matched by the product’s NDC code. A recall usually covers specific lots only: check the lot number on your package and ask your pharmacist. Do not stop a medicine on your own.

  1. September 16, 2015 · Class III · Terminated · D-0782-2016

    CGMP Deviations: Confirmed customer compliant of odor when turning on a cylinder of medical air.

    UN1002 Air, Compressed, Breathing Grade, USP, Distributed by Praxair Distribution, Inc. Roseville, MN 55113, NDC 59579-006. — Praxair Inc.

  2. March 10, 2015 · Class III · Terminated · D-0423-2015

    Failed Impurities/Degradation Specification; out of specification results for carbon dioxide

    AIR COMPRESSED, Medical Air, USP, Rx Only. Matheson Tri-Gas, Inc., 150 Allen Road, Basking Ridge, NJ 07920. Available in A) E or 22 cu ft cylinder, NDC: 55037-302-09; B) 40 cu ft cylinder, NDC: 55037-302-10; C) 200 cu ft — Matheson, Inc.

What do the recall classes mean?

Class I: The most serious type: there is a reasonable chance that using the product will cause serious health problems or death.
Class II: Using the product may cause temporary or medically reversible health problems, or the chance of serious problems is remote.
Class III: Using the product is not likely to cause health problems (for example a labeling or packaging issue).

Official identifiers

SPL set ID of the quoted labelfeb76dd5-9430-4df2-81c6-e4be48713c1b
FDA labels (SPL)9
FDA applicationsNDA205796, NDA205804, NDA205821, NDA205826, NDA205847, NDA205859, NDA205890, NDA205909, NDA205910, NDA207036
Active ingredients (FDA)AIR

Sources

  1. FDA-approved label on DailyMed (National Library of Medicine) — Air, Machine & Welding Supply Company dba Arc3 Gases South, effective December 2, 2025; via openFDA, FDA data exported October 30, 2026, retrieved October 31, 2026
  2. NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  3. Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  4. Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
  5. Drug shortages (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026

openFDA data is provided by the FDA as is; it may be incomplete. Always rely on the label that comes with your medicine. FDA Enforcement Report search →

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