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Prescription medicine

Carbon dioxide

Drug class: Radiographic Contrast Agent

The FDA’s “Established Pharmacologic Class”: the group of medicines that work in a similar way.

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 Carbon dioxide have a boxed warning?
No. None of the 36 FDA labels we found for this medicine has a boxed warning.
Is there a shortage of Carbon dioxide?
No current shortage is listed by the FDA for the products of this medicine (FDA data from October 30, 2026).
Has Carbon dioxide been recalled?
No recall linked to the products of this medicine appears in the FDA enforcement reports we use.
Who makes Carbon dioxide?
34 companies list prescription products of Carbon dioxide in the FDA NDC Directory, including Maine Oxy-Acetylene Supply Company, Roberts Oxygen Company, Inc. and General Air Service & Supply Co.

What Carbon dioxide 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 36 FDA labels for this medicine have a boxed warning.

Forms and how it is given

Dosage formsGas
RouteRespiratory (inhalation)
Prescription products40 in the FDA NDC Directory
Brand namesCarbon Dioxide Refrigerated

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
NDA205764
CARBON DIOXIDE, USP
Linde North America IncJuly 5, 2013 —
NDA205815
CARBON DIOXIDE, USP
Linde Merchant Productions IncJuly 5, 2013 —
NDA205846
CARBON DIOXIDE, USP
Airgas Carbonic IncJuly 20, 2013 —
NDA205852
CARBON DIOXIDE, USP
Praxair IncJuly 21, 2013 —
NDA206025
CARBON DIOXIDE, USP
Airgas USA LLCSeptember 7, 2013 —
NDA207166
CARBON DIOXIDE, USP
Reliant Holdings LtdMay 25, 2014 —
NDA213507
CARBON DIOXIDE, USP
A-Ox Welding Supply Co, Inc.June 15, 2019 —
NDA215007
CARBON DIOXIDE, USP
Nexair LLCJuly 18, 2020 —
NDA217082
CARBON DIOXIDE, USP
Continental Carbonic Products, Inc.February 25, 2022 —
NDA219303
CARBON DIOXIDE, USP
Haun Specialty Gases IncFebruary 17, 2024 —
NDA219779
CARBON DIOXIDE, USP
Central Welding SupplyAugust 10, 2024 —
NDA220050
Carbon Dioxide, USP
Djb Gas Services, IncNovember 9, 2024 —
NDA220266
Carbon Dioxide, USP
Welders Supply Company of Louisville IncFebruary 2, 2025 —
NDA220461
CARBON DIOXIDE, USP
Mitchell Wedling SupplyApril 21, 2025 —

Shortage status

The FDA drug shortage list does not show these products.

FDA Drug Shortages database →

Recalls

No recall linked to these products (by their NDC code) appears in the FDA enforcement reports.

Official identifiers

RxCUI (RxNorm)308998, 309002, 309004, 347023, 347024, 347967, 541999, 1091094, 1728767, 1790649
SPL set ID of the quoted label77f13272-8e40-8f92-92dd-dcb5aad0219d
FDA labels (SPL)36
FDA applicationsNDA205764, NDA205815, NDA205846, NDA205852, NDA206025, NDA207166, NDA213507, NDA215007, NDA217082, NDA219303, NDA219779, NDA220050, NDA220266, NDA220461
Active ingredients (FDA)CARBON DIOXIDE

Sources

  1. FDA-approved label on DailyMed (National Library of Medicine) — Carbon Dioxide Refrigerated, Messer LLC, effective February 16, 2026; 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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