FDA.reportPublic FDA data

OXYGEN

Manufacturer
CEE-KAY SUPPLY, INC.
Effective date
2026-02-25
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
17
Source
full-release
Hydrated at
2026-05-31 22:07:29

Label at a glance#

ProductOXYGEN
Active ingredientOXYGEN
Label structure3 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

OXYGEN, COMPRESSED USP

UN1072

WARNING: For emergency use only when administered by properly trained personnel for oxygen deficiency and resuscitation. For all other medical applications, Rx required. Uninterrupted use of high concentrations of oxygen over a long duration, without monitoring its effect on oxygen content of arterial blood, may be harmful. Do not attempt to use on patients who have stopped breathing unless used in conjunction with resuscitative equipment. Produced by Air Liquefaction. DANGER: MAY CAUSE OR INTENSIFY FIRE; OXIDIZER. CONTAINS GAS UNDER PRESSURE; MAY EXPLODE IF HEATED. Obtain, read and follow all safety instructions before use. Keep away from clothing and other combustible materials. Keep valves and fittings free from grease and oil. Use and store only outdoors or with adequate ventilation. Store in a well-ventilated place. In case of fire: Stop leak if safe to do so. Use a back flow preventive device in the piping. Use only equipment of compatible materials of construction and rated for cylinder pressure. Use only with equipment cleaned for oxygen service. Do not open valve until connected to equipment prepared for use. Open valve slowly. 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. CAS: 7782-44-7

DO NOT REMOVE THIS PRODUCT LABEL

CONTENTS: LTRS: CU.FT

CK SUPPLY CASES WELDING DRY ICE

5835 Manchester Avenue

St. Louis, MO 63110

(314) 644-3500

www.CKSupply.com

NO SMOKING

NO VAPING oxygen 2025oxygen 2025

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

OXYGEN, COMPRESSED USP

UN1072

PRODUCED BY AIR LIQUEFACTION

WARNING: For emergency use only when administered by properly trained personnel for deficiency and resuscitation. For all other medical applications, Rx required. Uninterrupted use of high concentrations of oxygen over a long duration, without monitoring its effect on oxygen content of arterial blood, may be harmful. Do not attempt to use on patients who have stopped breathing unless used in conjunction with resuscitative equipment.

DANGER: MAY CAUSE OR INTENSIFY FIRE; OXIDIZER. CONTAINS GAS UNDER PRESSURE; MAY EXPLODE IF HEATED. Obtain, read and follow all safety instructions before use. Keep away from clothing and other combustible materials. Keep valves and fittings free from grease and oil. Use and store only outdoors or with adequate ventilation. Store in a well-ventilated place. In case of fire: Stop leak if safe to do so. Use a back flow preventive device in the piping. Use only equipment of compatible materials of construction and rated for cylinder pressure. Use only with equipment cleaned for oxygen service. Do not open valve until connected to equipment prepared for use. Open valve slowly. 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. CAS: 7782-44-7 DO NOT REMOVE THIS PRODUCT LABEL.

CK SUPPLY CASES WELDING DRY ICE

5835 Manchester Avenue

St. Louis, MO 63110

(314) 644-3500

www.CKSupply.com

NO SMOKING

NO VAPING

CONTENTS: LTRS: CU.FT. oxygen two 2025oxygen two 2025

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

REFRIGERATED LIQUID

OXYGEN, REFRIGERATED LIQUID USP

UN1073

ALWAYS KEEP CONTAINER IN UPRIGHT POSITION.

DO NOT CHANGE OR FORCE FIT CONNECTIONS.

CONTENTS: LTRS: CU.FT

WARNING: For emergency use only when administered by properly trained personnel for oxygen deficiency and resuscitation. For all other medical applications, Rx required.

Uninterrupted use of high concentrations of oxygen over a long duration, without monitoring its effect on oxygen content of arterial blood, may be harmful. Do not attempt to use on patients who have stopped breathing unless used in conjunction with resuscitative equipment.

Produced by Air Liquefaction.

DANGER: MAY CAUSE OR INTENSIFY FIRE; OXIDIZER. CONTAINS REFRIGERATED GAS: MAY CAUSE CYROGENIC BURNS OR INJURY. COMBUSTIBLES IN CONTACT WITH OXIDIZING REFRIGERATED LIQUIDS MAY EXPLODE ON IGNITION OR IMPACT.

Obtain, read and follow all safety instructions before use. Keep away from clothing and other combustible materials. Keep valves and fittings free from grease and oil. Use only outdoors or with adequate ventilation. Store in a well-ventilated place. Wear cold insulating gloves and either face shield or eye protection. In case of fire: Stop leak if safe to do so. Use a back flow preventive device in the piping. Use only with equipment of compatible materials of construction and rated for cylinder pressure. Use only with equipment cleaned for oxygen service. DO NOT change or force fit connections. Avoid spills. Do not walk on or roll equipment over spills. Do not open valve until connected to equipment prepared for use. Open valve slowly. Close valve after each use and when empty. Always keep container in upright position. Read and follow the Safety Data Sheet (SDS) before use.

FIRST AID: IF ON SKIN: Thaw frosted parts with lukewarm water. Do not rub affected area. Get immediate medical help.

CAS: 7782-44-7

DO NOT REMOVE THIS PRODUCT LABEL.

CK SUPPLY CASES WELDING DRY ICE

5835 Manchester Avenue

St. Louis, MO 63110

(314) 644-3500

www.CKSupply.com

NO SMOKING

NO VAPING refrig oxygen 2025refrig oxygen 2025

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
312173oxygen 99.5 % Gas for InhalationPSN17
312173oxygen 99.5 % Gas for InhalationSCD17

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10218-001-01OXYGEN8500 L in 1 CYLINDERGAS850017
10218-001-02OXYGEN6000 L in 1 CYLINDERGAS600017
10218-001-03OXYGEN3000 L in 1 CYLINDERGAS300017
10218-001-04OXYGEN2000 L in 1 CYLINDERGAS200017
10218-001-05OXYGEN1000 L in 1 CYLINDERGAS100017
10218-001-06OXYGEN650 L in 1 CYLINDERGAS65017
10218-001-07OXYGEN400 L in 1 CYLINDERGAS40017
10218-001-08OXYGEN177 L in 1 DEWARGAS17717
10218-001-09OXYGEN146 L in 1 DEWARGAS14617
10218-001-10OXYGEN196 L in 1 DEWARGAS19617

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
OXYGENACTIVE INGREDIENTS88TT140655
OXYGENACTIVE MOIETYS88TT140655

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
10218-00110218-001-01, 10218-001-02, 10218-001-03, 10218-001-04, 10218-001-05, 10218-001-06, 10218-001-07, 10218-001-08, 10218-001-09, 10218-001-10

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
OXYGENS88TT14065ACTIB

Source Document#

Source XML · Source PDF

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
162025-11-17monthly-update2026-06-03 17:43:59

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
OXYGENOXYGENCEE-KAY SUPPLY, INC.7a4aa7ab-08a4-4e93-90d7-5329b0e1a61b2026-02-25Exact identifier
ndc (package): 10218-001-07
ndc (package): 10218-001-02
ndc (package): 10218-001-04
ndc (package): 10218-001-05
ndc (package): 10218-001-01
ndc (package): 10218-001-03
ndc (package): 10218-001-06
ndc (package): 10218-001-08
ndc (package): 10218-001-09
ndc (package): 10218-001-10
ndc (product): 10218-001
ndc11 (package): 10218000105
ndc11 (package): 10218000109
ndc11 (package): 10218000104
ndc11 (package): 10218000110
ndc11 (package): 10218000101
ndc11 (package): 10218000106
ndc11 (package): 10218000103
ndc11 (package): 10218000108
ndc11 (package): 10218000107
ndc11 (package): 10218000102
spl id: 4bae463f-cd7b-3ffd-e063-6294a90adb7a
spl set id: 7a4aa7ab-08a4-4e93-90d7-5329b0e1a61b

Reported adverse events (FAERS/openFDA)#

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