Carbon Dioxide

Manufacturer
Linde Gas & Equipment Inc.
Effective date
2021-12-14
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
8
Source
legacy-cache
Hydrated at
2026-08-01 22:21:00

Label at a glance#

ProductCarbon Dioxide
Active ingredientCarbon Dioxide
Label structure2 sections

Label contents#

Full prescribing information#

WARNINGS AND PRECAUTIONS SECTION

WARNING: Administration of Carbon Dioxide 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 Carbon Dioxide and is familiar with the indications, effects, dosages, methods and frequency and duration of administration, and the hazards, contraindications and side effects and the precautions to be taken. When used as a diluent for oxygen to produce respirable mixtures, user must assure sufficient oxygen concentration to sustain life.

WARNING: CONTAINS GAS UNDER PRESSURE: MAY EXPLODE IF HEATED. MAY DISPLACE OXYGEN AND CAUSE RAPID SUFFOCATION. MAY CAUSE FROSTBITE. MAY INCREASE RESPIRATION AND HEART RATE.
Do not handle until all safety precautions have been read an understood. Avoid breathing gas. Do not get in eyes, on skin, or on clothing. 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 cylinder pressure. Close valve after each use and whem empth. Protect from sunlight when ambient temperature exceeds 52°c (125°F). Read and follow the Safety Data Sheet (SDS) before use.

FIRST AID: IF INHALED: Remove person to fresh air and keep comfortable for breathing. Get medical advice/attention. IF ON SKIN: Thaw frosted parts with lukewarm water. Do not rub affected area. Get immediate medical advice/attention.

         

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CO2 Compressed Wall Label
CO2 Compressed Wall Label

Linde

CARBON DIOXIDE

USP

UN1013

CAS 124-38-9

2

MEDICAL GAS

RX ONLY.

DO NOT REMOVE THIS LABEL.

CONTENTS:
Cylinder
Type
 Liters
K[_]12367
M[_]7415
E[_]1472
D[_]991
______________________

Distributed by:
Linde Gas North America LLC
200 Somerset Corporate Blvd., Suite 7000
Bridgewater, NJ 08807
866.543.3427

LG030F

CO2 Compressed Shoulder Label
CO2 Compressed Shoulder Label

CARBON DIOXIDE

USP

UN1013

CAS 124-38-9

DO NOT REMOVE THIS PRODUCT LABEL.

2

MEDICAL GAS

RX ONLY

CONTENTS:
Cylinder
Type
 Liters
K[_]12367
M[_]7415
E[_]1472
D[_]991
______________________

Distributed by:
Linde Gas North America LLC
200 Somerset Corporate Blvd., Suite 7000
Bridgewater, NJ 08807
866.543.3427


MG011C

FDA-Initiated Inactive NDC Indexing#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
25373-004CARBON DIOXIDE (CARBON DIOXIDE) GAS [LINDE GAS & EQUIPMENT INC.]8Legacy NDC20211225_b4578d6a-296d-9650-a998-c86911590b4e.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
Carbon DioxideACTIVE INGREDIENT142M471B3J3
Carbon DioxideACTIVE MOIETY142M471B3J3

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
25373-00425373-004-01, 25373-004-02, 25373-004-03, 25373-004-04

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
Carbon Dioxide142M471B3JACTIB

Source Document#

Source XML

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
1deeb748-9898-4083-9629-22f26c62bb9db4578d6a-296d-9650-a998-c86911590b4e2025-12-18WarningsExact identifier
spl set id: b4578d6a-296d-9650-a998-c86911590b4e

Reported adverse events (FAERS/openFDA)#

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