FDA.reportPublic FDA data

Oxygen

Manufacturer
Hawaii Home Infusion Associates, Ltd.
Effective date
2025-11-24
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
18
Source
full-release
Hydrated at
2026-05-31 21:47:45

Label at a glance#

ProductOxygen
Active ingredientOXYGEN
Label structure1 sections

Label contents#

Full prescribing information#

Principal for Oxygen Product

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Representative LabelRepresentative Label

OXYGEN

COMPRESSED

USP

UN 1072

PRODUCED BY AIR LIQUIFICATION

WARNING: HIGH PRESSURE OXIDIZING GAS, VIGOROUSLY ACCELERATES COMBUSTION. NO SMOKING IN THE PRESENCE OF OXYGEN OR A FIRE MAY RESULT.

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

WARNING: Federal law prohibits dispensing without prescription. Uninterrupted use of high concentrations of oxygen over a long duration, without monitoring its effect on oxygen content of arterial blood, may be harmful. Use only with pressure reducing equipment and apparatus designed for oxygen. Do not attempt to use on patients who have stopped breathing, unless used in conjuction with resuscitative equipment.

WARNING: Keep oil and grease away. Use only with equipment cleaned for oxygen service and rated for cylinder pressure. Open valve slowly. Close valve after each use and when empty.

USE IN ACCORDANCE WITH MATERIAL SAFETY DATA SHEET.

DO NOT REMOVE THIS PRODUCT LABEL.

RepresentativeLotStickerRepresentativeLotSticker

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
312172oxygen 99 % Gas for InhalationPSN18
312172oxygen 99 % Gas for InhalationSCD18

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11401-6994-1Oxygen680 L in 1 CYLINDERGAS68018
11401-6994-2Oxygen415 L in 1 CYLINDERGAS41518
11401-6994-3Oxygen164 L in 1 CYLINDERGAS16418
11401-6994-4Oxygen1699 L in 1 CYLINDERGAS169918

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
OxygenACTIVE INGREDIENTS88TT140651
OxygenACTIVE MOIETYS88TT140651

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
11401-699411401-6994-2, 11401-6994-3, 11401-6994-1, 11401-6994-4

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

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
OxygenOXYGENHawaii Home Infusion Associates, Ltd.88b00c55-4200-4041-aabc-11fd431376ef2025-11-24Exact identifier
ndc (package): 11401-6994-4
ndc (package): 11401-6994-3
ndc (package): 11401-6994-1
ndc (package): 11401-6994-2
ndc (product): 11401-6994
ndc11 (package): 11401699403
ndc11 (package): 11401699402
ndc11 (package): 11401699404
ndc11 (package): 11401699401
spl id: 445e3177-c0b0-91c9-e063-6294a90a2d0f
spl set id: 88b00c55-4200-4041-aabc-11fd431376ef

Reported adverse events (FAERS/openFDA)#

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