FDA.reportPublic FDA data

Oxygen

Manufacturer
Home Care Equipment, Inc.
Effective date
2025-12-22
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
10
Source
full-release
Hydrated at
2026-05-31 21:52:15

Label at a glance#

ProductOxygen
Active ingredientOXYGEN
Label structure1 sections

Label contents#

Full prescribing information#

Principal for Oxygen Product

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

HPLabelHPLabel

OXYGEN,

COMPRESSED

USP

UN1072

C.A.S. NO. 7782-44-7

OXYGEN

2

HOME CARE EQUIPMENT INC.

1700 WEST HARPER ST

POPLAR BLUFF, MO 63901

800-457-4131

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. Keep out of reach of children. Federal law requires that this container be refilled with oxygen USP only by establishments registered as a drug manufacturer in accordance with the Federal Food, Drug and Cosmetic Act.

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 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. Close valve after each use and when empty. Use only with equipment rated for cylinder pressure. Do not open valve until connected to equipment prepared for use. Use only equipment of compatible materials of construction. Open valve slowly. Use only with equipment cleaned for oxygen service. Protect from sunlight when ambient temperature exceeds 52°C (125°F). Read and follow the Safety Data Sheet (SDS) before use.

NO SMOKING

NO VAPING

Size / Contents

☐ M6 — 170 Liters

☐ D — 415 Liters

☐ E — 682 Liters

☐ M — 2840 Liters

☐ H — 6910 Liters

☐ Other ______ Liters

DO NOT REMOVE THIS PRODUCT LABEL

RepresentativeLotStickerRepresentativeLotSticker

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
312172oxygen 99 % Gas for InhalationPSN10
312172oxygen 99 % Gas for InhalationSCD10

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
57959-123-01Oxygen21.1 L in 1 DEWARGAS21.110
57959-123-04Oxygen170 L in 1 CYLINDERGAS17010
57959-123-05Oxygen415 L in 1 CYLINDERGAS41510
57959-123-06Oxygen682 L in 1 CYLINDERGAS68210
57959-123-08Oxygen6910 L in 1 CYLINDERGAS691010
57959-123-09Oxygen45 L in 1 DEWARGAS4510
57959-123-10Oxygen60 L in 1 DEWARGAS6010
57959-123-11Oxygen145 L in 1 DEWARGAS14510
57959-123-12Oxygen3455 L in 1 CYLINDERGAS345510

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
57959-12357959-123-04, 57959-123-05, 57959-123-06, 57959-123-08, 57959-123-10, 57959-123-11, 57959-123-12, 57959-123-01, 57959-123-09

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
OxygenOXYGENHome Care Equipment, Inc.25ef3128-6b28-3c20-e054-00144ff8d46c2025-12-22Exact identifier
ndc (package): 57959-123-10
ndc (package): 57959-123-01
ndc (package): 57959-123-05
ndc (package): 57959-123-11
ndc (package): 57959-123-12
ndc (package): 57959-123-08
ndc (package): 57959-123-09
ndc (package): 57959-123-06
ndc (package): 57959-123-04
ndc (product): 57959-123
ndc11 (package): 57959012310
ndc11 (package): 57959012308
ndc11 (package): 57959012311
ndc11 (package): 57959012305
ndc11 (package): 57959012309
ndc11 (package): 57959012312
ndc11 (package): 57959012306
ndc11 (package): 57959012301
ndc11 (package): 57959012304
spl id: 468df563-ae41-df2e-e063-6394a90ad5ca
spl set id: 25ef3128-6b28-3c20-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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