OXYGEN

Manufacturer
Johnson Drug Company, Inc
Effective date
2025-11-21
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
9
Source
full-release
Hydrated at
2026-05-31 21:46:53

Label at a glance#

ProductOXYGEN
Active ingredientOXYGEN
Label structure1 sections

Label contents#

Full prescribing information#

OXYGEN COMPRESSED USP product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

OXYGEN COMPRESSED USP       UN 1072       OXYGEN-2

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 the ambient temperature exceeds 52° C ( 125° F). Read and follow the Safety Data Sheet (SDS) before use.

DO NOT REMOVE THIS PRODUCT LABEL.

WARNING: For emergency use only when administered by properly trained personnel for oxygen defiiciency 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 withresuscitative equipment. Produced by Air Liquefaction. ©Applied Home Healthcare Equipment 2014

CAS NO: 7782-44-7

Contents           Size

113 Liters          M4

165 Liters          M6

255 Liters          C

425 Liters          D

680 Liters          E

7080 Liters        H

____ Liters        Other

Johnson Drug Co & Home Medical Inc

714 New Bridge Street

Jacksonville, NC 28540

910-347-5185

JohnsonOxygenJohnsonOxygen

res

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
64763-099-01OXYGEN175 L in 1 CYLINDERGAS1759
64763-099-02OXYGEN450 L in 1 CYLINDERGAS4509
64763-099-03OXYGEN675 L in 1 CYLINDERGAS6759

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
64763-09964763-099-01, 64763-099-02, 64763-099-03

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 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
OXYGENOXYGENJohnson Drug Company, Inc1b7bb66c-b4a2-48d9-a7df-373149da678c2025-11-21Exact identifier
ndc (package): 64763-099-01
ndc (package): 64763-099-02
ndc (package): 64763-099-03
ndc (product): 64763-099
ndc11 (package): 64763009903
ndc11 (package): 64763009901
ndc11 (package): 64763009902
spl id: d677a1d9-afd1-495c-bd20-ff009a8f9d40
spl set id: 1b7bb66c-b4a2-48d9-a7df-373149da678c

Reported adverse events (FAERS/openFDA)#

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