FDA.reportPublic FDA data

Carbon Dioxide

Manufacturer
Linde Gas & Equipment Inc.
Effective date
2021-12-14
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 22:20:53

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 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, contraindication and side effects and the precautions to be taken.

WARNING: CONTAINS REFRIGERATED GAS; MAY CAUSE CRYOGENIC BURNS OR INJURY. MAY DISPLACE OXYGEN AND CAUSE RAPID SUFFOCATION. MAY INCREASE RESPIRATION AND HEART RATE.

Do not handle until all safety precautions have been read and understood. Use and store only outdoors or in a well-ventilated place. Wear cold insulating gloves, face shield, and eye protection. Use a back flow preventive device in the piping. DO NOT change or force fit connections. Close valve after each use and when empty. Always keep container in upright position. Read and follow the Safety Data Sheet (SDS) before use.
 

       

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CO2 Liquid Wall Label
CO2 Liquid Wall Label

Linde

CARBON DIOXIDE, REFRIGERATED LIQUID

USP

UN2187

CAS 124-38-9

2

MEDICAL GAS

ALWAYS KEEP CONTAINER IN UPRIGHT POSITION

DO NOT CHANGE OR FORCE FIT CONNECTIONS

Rx Only

FIRST AID

IF INHALED: Remove person to fresh air and keep comfortable for breathing.

IF ON SKIN: Thaw frosted parts with lukewarm water. Do not rub affected area. Get immediate medical advice/attention.

DO NOT REMOVE THIS LABEL

WARNING: USE OF ADAPTORS IS PROHIBITED

WARNING: DO NOT REMOVE FITTINGS

CONTENTS:
Cylinder
Type		Liters  
160L91905[_]
180L102282[_]
200L108705[_]
230L130447[_]
_____________________

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

LG031F

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
25373-104-052025-12-19C16284748780-1f386c64a-2751-0266-e053-dadaa90a7c1aCARBON DIOXIDE, REFRIGERATED LIQUID
25373-104-062025-12-19C16284748780-1f386c64a-2751-0266-e053-dadaa90a7c1aCARBON DIOXIDE, REFRIGERATED LIQUID
25373-104-072025-12-19C16284748780-1f386c64a-2751-0266-e053-dadaa90a7c1aCARBON DIOXIDE, REFRIGERATED LIQUID
25373-104-082025-12-19C16284748780-1f386c64a-2751-0266-e053-dadaa90a7c1aCARBON DIOXIDE, REFRIGERATED LIQUID
25373-104-052023-01-30C16284748780-1f386c64a-2751-0266-e053-dadaa90a7c1aCARBON DIOXIDE, REFRIGERATED LIQUID
25373-104-062023-01-30C16284748780-1f386c64a-2751-0266-e053-dadaa90a7c1aCARBON DIOXIDE, REFRIGERATED LIQUID
25373-104-072023-01-30C16284748780-1f386c64a-2751-0266-e053-dadaa90a7c1aCARBON DIOXIDE, REFRIGERATED LIQUID
25373-104-082023-01-30C16284748780-1f386c64a-2751-0266-e053-dadaa90a7c1aCARBON DIOXIDE, REFRIGERATED LIQUID

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
25373-104CARBON DIOXIDE (CARBON DIOXIDE) GAS [LINDE GAS & EQUIPMENT INC.]5Legacy NDC20211225_06b0e5d9-c33d-8376-465b-f29fa3d545e5.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
Carbon DioxideACTIVE INGREDIENT142M471B3J2
Carbon DioxideACTIVE MOIETY142M471B3J2

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
25373-10425373-104-05, 25373-104-06, 25373-104-07, 25373-104-08

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
3c02b3ca-db7a-474a-8c5a-3c7fc06211f806b0e5d9-c33d-8376-465b-f29fa3d545e52025-12-19WarningsExact identifier
spl set id: 06b0e5d9-c33d-8376-465b-f29fa3d545e5

Reported adverse events (FAERS/openFDA)#

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