Oxygen

Manufacturer
KTL&C LLC dba RX Positive Medical Supply
Effective date
2025-10-21
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
9
Source
full-release
Hydrated at
2026-05-31 22:02:36

Label at a glance#

ProductOxygen
Active ingredientOXYGEN
Label structure1 sections

Label contents#

Full prescribing information#

Principal for Oxygen Product

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

RepresentativeHPLabelRepresentativeHPLabel

OXYGEN

COMPRESSED

USP

UN 1072

DANGER:

MAY CAUSE OR INTENSIFY FIRE; OXIDIZER. CONTAINS GAS UNDER PRESSURE; MAY EXPLODE IF HEATED.
Do not handle until all safety precautions have been read and understood. Keep and store away from clothing and other combustible materials. Keep valves and fittings free from grease and oil. Use and store only outdoors or 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 with equipment of compatible materials of construction and rated for cylinder pressure. Use only with equipment cleaned for oxygen service. 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 NO: 7782-44-7

DO NOT REMOVE THIS PRODUCT LABEL.

WARNING: No smoking or vaping. For emergency use only when administered by properly trained personnel for oxygen deficiency

and resuscitation. For all other medical applications, Rx only.

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.

RepresentativeLotStickerRepresentativeLotSticker

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
312172oxygen 99 % Gas for InhalationPSN9
312172oxygen 99 % Gas for InhalationSCD9

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
14080-001-01Oxygen164 L in 1 CYLINDERGAS1649
14080-001-02Oxygen255 L in 1 CYLINDERGAS2559
14080-001-03Oxygen425 L in 1 CYLINDERGAS4259
14080-001-04Oxygen640 L in 1 CYLINDERGAS6409
14080-001-05Oxygen680 L in 1 CYLINDERGAS6809
14080-001-06Oxygen3455 L in 1 CYLINDERGAS34559
14080-001-07Oxygen7080 L in 1 CYLINDERGAS70809

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
14080-00114080-001-01, 14080-001-02, 14080-001-03, 14080-001-04, 14080-001-05, 14080-001-06, 14080-001-07

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

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
82024-11-19full-release2026-05-31 21:17:41

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
OxygenOXYGENKTL&C LLC dba RX Positive Medical Supply857dae8d-ffeb-19fd-e053-2a91aa0a8dcf2025-10-21Exact identifier
ndc (package): 14080-001-04
ndc (package): 14080-001-01
ndc (package): 14080-001-05
ndc (package): 14080-001-06
ndc (package): 14080-001-03
ndc (package): 14080-001-02
ndc (package): 14080-001-07
ndc (product): 14080-001
ndc11 (package): 14080000107
ndc11 (package): 14080000106
ndc11 (package): 14080000104
ndc11 (package): 14080000103
ndc11 (package): 14080000102
ndc11 (package): 14080000101
ndc11 (package): 14080000105
spl id: 41b0a444-5c47-096c-e063-6294a90a13ca
spl set id: 857dae8d-ffeb-19fd-e053-2a91aa0a8dcf

Reported adverse events (FAERS/openFDA)#

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