Oxygen

Manufacturer
HELGET, INC. | HELGET, INC. dba Helget Home Care Capital Medical
Effective date
2025-12-09
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-05-31 21:49:23

Label at a glance#

ProductOxygen
Active ingredientOXYGEN
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

OXYGEN, REFRIGERATED LIQUID USP
UN 1073
CAS: 7782-44-7
PRODUCED BY AIR LIQUEFACTION
ALWAYS KEEP CONTAINER IN UPRIGHT POSITION
DANGER
Rx only
MAY CAUSE OR INTENSIFY FIRE; OXIDIZER. CONTAINS REFRIGERATED GAS; MAY CAUSE CRYOGENIC BURNS OR INJURY. COMBUSTIBLES IN CONTACT WITH LIQUID OXYGEN MAY EXPLODE ON IGNITION OR IMPACT. KEEP OUT OF REACH OF CHILDREN.
Caution: Do not handle until all safety precautions have been read and understood. Keep/Store away from clothing, combustible materials. Keep reduction valves/valves and fittings free from oil and grease. Use and store only outdoors or in a well-ventilated place. Wear cold insulating gloves, face shield, 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 spill. Do not walk on or roll equipment over spills. Always keep container in upright position. Use in accordance with Safety Data Sheet for this product.
First Aid: IF ON SKIN; Thaw frosted parts with lukewarm water. Do not rub affected area. Get immediate medical advice/attention.
Warning: 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.
DO NOT REMOVE THIS LABEL
HELGET HOME CARE
8609 F ST., OMAHA, NE 68127
402-339-1054 image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
312175oxygen 99.9 % Gas for InhalationPSN5
312175oxygen 99.9 % Gas for InhalationSCD5

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
26124-002-01Oxygen41 L in 1 CYLINDERGAS415
26124-002-02Oxygen21 L in 1 CYLINDERGAS215
26124-002-03Oxygen46 L in 1 CYLINDERGAS465

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
26124-00226124-002-01, 26124-002-02, 26124-002-03
52086-011

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

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 · 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
OxygenOXYGENHelget Gas Productsf791c94b-7fba-3857-e053-6294a90ac6be2025-12-19Exact identifier
ndc (product): 52086-011
OxygenOXYGENHELGET, INC.fc4d37c6-d6a1-24ef-e053-6394a90a8b0f2025-12-09Exact identifier
ndc (package): 26124-002-01
ndc (package): 26124-002-03
ndc (package): 26124-002-02
ndc (product): 26124-002
ndc11 (package): 26124000203
ndc11 (package): 26124000201
ndc11 (package): 26124000202
spl id: 458a037a-520a-cd0b-e063-6394a90ad163
spl set id: fc4d37c6-d6a1-24ef-e053-6394a90a8b0f

Reported adverse events (FAERS/openFDA)#

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