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Carbon Dioxide-Oxygen Mixture

Prescription NDA
Informational index, not medical advice. Content is reproduced from public FDA and NLM data. Always confirm against the manufacturer's current prescribing information. Report adverse events to FDA MedWatch.

Overview

Brand name
Carbon Dioxide-Oxygen Mixture
Generic name
Carbon Dioxide-Oxygen Mixture
Dosage form
Gas
Route
Respiratory (Inhalation)
Marketing category
NDA · NDA
Labeler
Roberts Oxygen Company, Inc.
Product type
Human Prescription Drug
DEA schedule
Not scheduled
Active ingredients
12
NDC product codes
6
Packages
12
Data completeness
52% of corroborating sources present

Active ingredients

Source: NDC Directory
Active ingredients and strengths as listed in the NDC Directory.
Ingredient Strength RxCUI Monograph
Carbon Dioxide 100 mL/L 308998 View
Carbon Dioxide 120 mL/L 308998 View
Carbon Dioxide 150 mL/L 308998 View
Carbon Dioxide 200 mL/L 308998 View
Carbon Dioxide 50 mL/L 308998 View
Carbon Dioxide 70 mL/L 308998 View
Oxygen 800 mL/L 312172 View
Oxygen 850 mL/L 312172 View
Oxygen 880 mL/L 312172 View
Oxygen 900 mL/L 312172 View
Oxygen 930 mL/L 312172 View
Oxygen 950 mL/L 312172 View

Forms, strengths and routes

Source: NDC Directory
Dosage form
Gas
Route of administration
Respiratory (Inhalation)
Presentations
18

Pharmacologic classes are listed in the class section below.

Pharmacologic class

Source: NDC Directory
Established pharmacologic classes (EPC), mechanisms of action (MoA), chemical structures (CS) and physiologic effects (PE).
Class Type Browse
Radiographic Contrast Agent [EPC] EPC All 19 members
X-Ray Contrast Activity [MoA] MoA All 19 members

Regulatory status

Source: Drugs@FDANDC Directory
Application number
205849
Application type
NDA · New Drug Application
Approval date
July 21, 2013
Sponsor
PRAXAIR INC
Products on application
1
Submissions recorded
1
Products approved under application 205849.
Product Trade name Form Strength Ingredient Status TE Flags
205849-001 OXYGEN, USP GAS OXYGEN Prescription —

Approval history

Source: Drugs@FDA
Most recent submissions on application 205849.
Type No. Action Status Date Review
Original application 1 Medical Gas Approved July 21, 2013 Standard

Review documents

  • 0 · Original application · September 30, 2015

Adverse event reports

Source: openFDA FAERS
48,982
FAERS reports mentioning this drug
as of 2026-09-25T03:42:24+00:00
A report count is not a risk measure. FAERS accepts voluntary and mandatory reports without establishing causation, and reporting is influenced by how widely a drug is used, how long it has been marketed, and media attention. FDA states that reports “do not prove that the drug caused the event”. Compare rates, not totals.

Attributed to this product's most-reported active ingredient: OXYGEN. Combination products with more than six active ingredients are not attributed, because a report count summed across a long ingredient list measures the list, not the medicine.

Packaging and NDCs

Source: NDC Directory
Every National Drug Code package associated with this medication. The NDC is the identifier used for dispensing, billing and pharmacovigilance in the United States.
Package NDC Product NDC Labeler Description Marketing start
46123-120-01 46123-120 Roberts Oxygen Company, Inc. 641 L in 1 CYLINDER (46123-120-01) January 1, 1966
46123-123-01 46123-123 Roberts Oxygen Company, Inc. 648 L in 1 CYLINDER (46123-123-01) January 1, 1966
46123-124-01 46123-124 Roberts Oxygen Company, Inc. 656 L in 1 CYLINDER (46123-124-01) January 1, 1966
46123-124-02 46123-124 Roberts Oxygen Company, Inc. 6521 L in 1 CYLINDER (46123-124-02) January 1, 1966
46123-124-03 46123-124 Roberts Oxygen Company, Inc. 7193 L in 1 CYLINDER (46123-124-03) January 1, 1966
46123-521-01 46123-521 Roberts Oxygen Company, Inc. 641 L in 1 CYLINDER (46123-521-01) January 1, 1966
46123-521-02 46123-521 Roberts Oxygen Company, Inc. 2210 L in 1 CYLINDER (46123-521-02) January 1, 1966
46123-521-03 46123-521 Roberts Oxygen Company, Inc. 6371 L in 1 CYLINDER (46123-521-03) January 1, 1966
46123-522-01 46123-522 Roberts Oxygen Company, Inc. 641 L in 1 CYLINDER (46123-522-01) January 1, 1966
46123-522-02 46123-522 Roberts Oxygen Company, Inc. 6371 L in 1 CYLINDER (46123-522-02) January 1, 1966
46123-911-01 46123-911 Roberts Oxygen Company, Inc. 708 L in 1 CYLINDER (46123-911-01) January 1, 1966
46123-911-02 46123-911 Roberts Oxygen Company, Inc. 6934 L in 1 CYLINDER (46123-911-02) January 1, 1966
46123-120 46123-120 Roberts Oxygen Company, Inc. — January 1, 1966
46123-123 46123-123 Roberts Oxygen Company, Inc. — January 1, 1966
46123-124 46123-124 Roberts Oxygen Company, Inc. — January 1, 1966
46123-521 46123-521 Roberts Oxygen Company, Inc. — January 1, 1966
46123-522 46123-522 Roberts Oxygen Company, Inc. — January 1, 1966
46123-911 46123-911 Roberts Oxygen Company, Inc. — January 1, 1966

Sources for this page

Every dataset that contributed a fact to this page.
Dataset Agency Used for
NDC Directory FDA Identity, ingredients, strengths, forms, routes, labelers, packages
Drugs@FDA FDA Application, sponsor, submissions, review documents, marketing status
FAERS FDA Adverse event report counts

Generated September 25, 2026 · 9 sections on this page.