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Carbon Dioxide-Air 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-Air Mixture
Generic name
Carbon Dioxide-Air 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
5
NDC product codes
4
Packages
11
Data completeness
46%
of corroborating sources present
Active ingredients
Source: NDC DirectoryForms, strengths and routes
Source: NDC DirectoryDosage form
Gas
Route of administration
Respiratory (Inhalation)
Presentations
15
Pharmacologic classes are listed in the class section below.
Pharmacologic class
Source: NDC Directory| 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 DirectoryApplication number
205849
Application type
NDA · New Drug Application
Approval date
July 21, 2013
Sponsor
PRAXAIR INC
Products on application
1
Submissions recorded
1
| Product | Trade name | Form | Strength | Ingredient | Status | TE | Flags |
|---|---|---|---|---|---|---|---|
| 205849-001 | OXYGEN, USP | GAS | OXYGEN | Prescription | — |
Approval history
Source: Drugs@FDA| 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 FAERS48,982
FAERS reports mentioning this drug
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| Package NDC | Product NDC | Labeler | Description | Marketing start |
|---|---|---|---|---|
| 46123-016-01 | 46123-016 | Roberts Oxygen Company, Inc. | 6060 L in 1 CYLINDER (46123-016-01) | January 1, 1966 |
| 46123-115-01 | 46123-115 | Roberts Oxygen Company, Inc. | 651 L in 1 CYLINDER (46123-115-01) | January 1, 1966 |
| 46123-115-02 | 46123-115 | Roberts Oxygen Company, Inc. | 991 L in 1 CYLINDER (46123-115-02) | January 1, 1966 |
| 46123-115-03 | 46123-115 | Roberts Oxygen Company, Inc. | 5405 L in 1 CYLINDER (46123-115-03) | January 1, 1966 |
| 46123-115-04 | 46123-115 | Roberts Oxygen Company, Inc. | 6060 L in 1 CYLINDER (46123-115-04) | January 1, 1966 |
| 46123-115-05 | 46123-115 | Roberts Oxygen Company, Inc. | 6900 L in 1 CYLINDER (46123-115-05) | January 1, 1966 |
| 46123-117-01 | 46123-117 | Roberts Oxygen Company, Inc. | 6060 L in 1 CYLINDER (46123-117-01) | January 1, 1966 |
| 46123-117-02 | 46123-117 | Roberts Oxygen Company, Inc. | 6200 L in 1 CYLINDER (46123-117-02) | January 1, 1966 |
| 46123-181-01 | 46123-181 | Roberts Oxygen Company, Inc. | 680 L in 1 CYLINDER (46123-181-01) | January 1, 1966 |
| 46123-181-02 | 46123-181 | Roberts Oxygen Company, Inc. | 2209 L in 1 CYLINDER (46123-181-02) | January 1, 1966 |
| 46123-181-03 | 46123-181 | Roberts Oxygen Company, Inc. | 6088 L in 1 CYLINDER (46123-181-03) | January 1, 1966 |
| 46123-016 | 46123-016 | Roberts Oxygen Company, Inc. | — | January 1, 1966 |
| 46123-115 | 46123-115 | Roberts Oxygen Company, Inc. | — | January 1, 1966 |
| 46123-117 | 46123-117 | Roberts Oxygen Company, Inc. | — | January 1, 1966 |
| 46123-181 | 46123-181 | Roberts Oxygen Company, Inc. | — | January 1, 1966 |
Sources for 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.