Oxygen

Manufacturer
Messer Gas Puerto Rico, Inc
Effective date
2025-11-18
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
14
Source
full-release
Hydrated at
2026-05-31 21:46:29

Label at a glance#

ProductOxygen
Active ingredientOXYGEN
Label structure2 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Certificate of Analysis – Oxygen USP

Product:
Oxygen USP

Date

Facility Name

Facility Address

Lot #

Batch #

Final Analysis Results

Analyzer #

Test / Units

USP Specs

Analysis Results

N/A

Odor

None

% O₂

≥99.0%

%

(Messer Spec ≥99.50%)

ppm H₂O

N/A

ppm

ppm THC

N/A

ppm

N/A

% CO

≤ .001

***

N/A

% CO₂

≤ .03

***

NT = not tested
*** = This product was manufactured by Air Liquefaction and testing is exempt under the USP compendium.

The methodology used to perform the USP test:

Paramagnetic Analyzer Manufacturer/Model #:

This analyzer has been validated by Messer as acceptable alternatives to the official USP for Oxygen Assay.
Validation study documentation is maintained by Messer at the corporate offices.

Analyst

Date

Quality Reviewer

Date

Should the material not be delivered to a USP customer, the material is “Not Approved for Human Drug Use.” Oxygen Refrigerated Liquid COAOxygen Refrigerated Liquid COA

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Certificate of Analysis – Oxygen USP

Product:
Oxygen USP

Date

Facility Name

Facility Address

Lot #

NDA

205818

Batch #

NADA 141374

Final Analysis Results

Analyzer #

Test / Units

USP Specs

Analysis Results

N/A

Odor

None

% O₂

≥99.0%

%

(Messer Spec ≥99.50%)

ppm H₂O

N/A

ppm

ppm THC

N/A

ppm

N/A

% CO

≤ .001

***

N/A

% CO₂

≤ .03

***

NT = not tested
*** = This product was manufactured by Air Liquefaction and testing is exempt under the USP compendium.

The methodology used to perform the USP test:

Paramagnetic Analyzer Manufacturer/Model #:

This analyzer has been validated by Messer as acceptable alternatives to the official USP for Oxygen Assay.
Validation study documentation is maintained by Messer at the corporate offices.

Analyst

Date

Quality Reviewer

Date

Should the material not be delivered to a USP customer, the material is “Not Approved for Human Drug Use.” oxygen pr 2025oxygen pr 2025

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
312172oxygen 99 % Gas for InhalationPSN14
312172oxygen 99 % Gas for InhalationSCD14

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52374-101-01Oxygen160 L in 1 DEWARGAS16014
52374-101-02Oxygen180 L in 1 DEWARGAS18014
52374-101-03Oxygen200 L in 1 DEWARGAS20014
52374-101-04Oxygen230 L in 1 DEWARGAS23014
52374-101-05Oxygen45 L in 1 DEWARGAS4514
52374-101-06Oxygen52 L in 1 DEWARGAS5214

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
OxygenACTIVE INGREDIENTS88TT140656
OxygenACTIVE MOIETYS88TT140656

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
52374-10152374-101-01, 52374-101-02, 52374-101-03, 52374-101-04, 52374-101-05, 52374-101-06

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
OxygenOXYGENMesser Gas Puerto Rico, Inccbb96c08-7ebc-2f30-cb54-73916fdb87d72025-11-18Exact identifier
ndc (package): 52374-101-03
ndc (package): 52374-101-06
ndc (package): 52374-101-05
ndc (package): 52374-101-04
ndc (package): 52374-101-02
ndc (package): 52374-101-01
ndc (product): 52374-101
ndc11 (package): 52374010104
ndc11 (package): 52374010103
ndc11 (package): 52374010101
ndc11 (package): 52374010106
ndc11 (package): 52374010105
ndc11 (package): 52374010102
spl id: 43e1d859-acfa-f299-e063-6294a90a49c2
spl set id: cbb96c08-7ebc-2f30-cb54-73916fdb87d7

Reported adverse events (FAERS/openFDA)#

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