FDA.reportPublic FDA data

Carbon Dioxide-Air Mixture

Manufacturer
Roberts Oxygen Company, Inc.
Effective date
2025-11-17
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
7
Source
full-release
Hydrated at
2026-05-31 21:46:28

Label at a glance#

ProductCarbon Dioxide-Air Mixture
Active ingredientCARBON DIOXIDE, OXYGEN
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

COMPRESSED GAS, N.O.S.
(% AIR, USP % CARBON DIOXIDE, USP)
UN1956
Rx only. WARNING: Administration of this gas mixture may be hazardous or contraindicated. For use only by or under the supervision of a licensed practitioner who is experienced in the use and administration of gas mixtures, and if familiar with the indications, effects, dosages, methods, and frequency and duration of administration, and with the hazards, contraindications and side effects, and the precautions to be taken. WARNING: CONTAINS GAS UNDER PRESSURE; MAY EXPLODE IF HEATED. MAY INCREASE RESPIRATION AND HEARTRATE. MAY DISPLACE OXYGEN AND CAUSE RAPID SUFFOCATION. Do not handle until all safety precautions have been read and understood.
Use and store only outdoors or in a well-ventilated place. Use a back flow preventive device in the piping. Use only with equipment rated for the cylinder pressure. Close valve after each use and when empty. Protect from sunlight when ambient temperature exceeds 52 C (125 F). Read and follow the Safety Data Sheet (SDS) before use. FIRST AID: IF ACCIDENTALLY INHALED: Remove person to fresh air and keep comfortable for breathing. Get medical advice/attention.
CAS: AIR 132259-10-0, CARBON DIOXIDE 124-38-9 DO NOT REMOVE THIS PRODUCT LABEL.
Roberts Oxygen Company, Inc.
PO Box 5507 Rockville, MD 20855
301-948-8100 air carbon dioxide mixair carbon dioxide mix

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
999632carbon dioxide 8 % / oxygen 21 % Gas for InhalationPSN7
999632carbon dioxide 8 % / oxygen 21 % Gas for InhalationSCD7
999632carbon dioxide 8 % / medical air (nitrogen 71 % / oxygen 21 % ) Gas for InhalationSY7

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
CARBON DIOXIDE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
46123-117-01Carbon Dioxide-Air Mixture6060 L in 1 CYLINDERGAS60607
46123-117-02Carbon Dioxide-Air Mixture6200 L in 1 CYLINDERGAS62007

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
46123-11746123-117-01, 46123-117-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
NITROGENN762921K75IACT
CARBON DIOXIDE142M471B3JACTIB
OXYGENS88TT14065ACTIB

Source Document#

Source XML

Orange Book application contexts#

All distinct exact application/product contexts derived from this label’s complete NDC list are paginated below.

Orange Book application contexts page 1 of 1 · 1 matching rows.

Source provenance: Browse the complete Orange Book source catalog.

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Carbon Dioxide-Air MixtureCARBON DIOXIDE-AIR MIXTURERoberts Oxygen Company, Inc.be034e3c-526f-41cb-bfa0-88883232ea9b2025-11-17Exact identifier
ndc (package): 46123-117-01
ndc (package): 46123-117-02
ndc (product): 46123-117
ndc11 (package): 46123011702
ndc11 (package): 46123011701
spl id: 43cf2bd4-733c-7271-e063-6394a90a550c
spl set id: be034e3c-526f-41cb-bfa0-88883232ea9b

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.