FDA.reportPublic FDA data

CARBON DIOXIDE

Manufacturer
Sexton Weldilng Supply Co., Inc.
Effective date
2010-01-01
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:52:50

Label at a glance#

ProductCARBON DIOXIDE
Active ingredientCARBON DIOXIDE
Label structure2 sections

Label contents#

Full prescribing information#

CARBON DIOXIDE USP LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CARBON DIOXIDE USP UN 1013 Rx ONLY NON-FLAMMABLE GAS-2

Rx ONLY  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 WITH THE HAZARDS AND CONTRAINDICATIONS AND SIDE EFFECTS AND THE PRECAUTIONS TO BE TAKEN. 

CHEMTREC EMERGENCY HOTLINE 1-800-424-9300

SWS-23 DO NOT REMOVE THIS PRODUCT LABEL

CO2 LABELCO2 LABEL

PRODUCT WARNINGS AND PRECAUTIONS

WARNINGS AND PRECAUTIONS SECTION

CAUTION: HIGH PRESSURE LIQUID AND GAS.  CAN CAUSE RAPID SUFFOCATION.  CAN INCREASE RESPIRATION AND HEART RATE.  MAY CAUSE FROSTBITE.  AVOID BREATHING GAS.  STORE AND USE WITH ADEQUATE VENTILATION.  DO NOT GET LIQUID IN EYES ON SKIN OR CLOTHING.  CYLINDER TEMPERATURE SHOULD NOT EXCEED 52 C (125 F)  USE EQUIPMENT RATED FOR CYLINDER PRESSURE.  CLOSE VALVE AFTER EACH USE AND WHEN EMPTY.  USE IN ACCORDANCE WITH MATERIAL SAFETY DATA SHEETS.  NOTE: SUCK-BACK INTO CYLINDER MAY CAUSE RUPTURE.  ALWAYS USE A BACK FLOW PREVENTATIVE DEVICE IN THE PIPING. 

FIRST AID: IF INHALED REMOVE TO FRESH AIR.  IF NOT BREATHING GIVE ARTIFICIAL RESPIRATION.  IF BREATHING IS DIFFICULT GIVE OXYGEN.  CALL A PHYSICIAN.  IN CASE OF FROSTBITE OBTAIN MEDICAL TREATMENT IMMEDIATELY.

DO NOT REMOVE THIS PRODUCT LABEL.

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
43861-1013-12022-04-01C16284748780-19d75b9d0-2fe3-f424-e053-dadaa90a57ce93ab91c5-1d9c-48e6-9b88-264c805ec39e
43861-1013-22022-04-01C16284748780-19d75b9d0-2fe3-f424-e053-dadaa90a57ce93ab91c5-1d9c-48e6-9b88-264c805ec39e
43861-1013-12020-01-31C16284748780-19d75b9d0-2fe3-f424-e053-dadaa90a57ce93ab91c5-1d9c-48e6-9b88-264c805ec39e
43861-1013-22020-01-31C16284748780-19d75b9d0-2fe3-f424-e053-dadaa90a57ce93ab91c5-1d9c-48e6-9b88-264c805ec39e

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
CARBON DIOXIDEACTIVE INGREDIENT142M471B3J1
CARBON DIOXIDEACTIVE MOIETY142M471B3J1

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
43861-101343861-1013-1, 43861-1013-2

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
db9bc6ae-4e7e-87e3-e053-2a95a90a957693ab91c5-1d9c-48e6-9b88-264c805ec39e2022-03-29WarningsExact identifier
spl set id: 93ab91c5-1d9c-48e6-9b88-264c805ec39e

Reported adverse events (FAERS/openFDA)#

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