NITROGEN

Manufacturer
PURITY CYLINDER GASES INC
Effective date
2018-10-31
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
12
Source
full-release
Hydrated at
2026-05-31 20:26:42

Label at a glance#

ProductNITROGEN
Active ingredientNITROGEN
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NITROGEN REFRIGERATED LIQUID NF
UN 1977
ALWAYS KEEP CONTAINER IN UPRIGHT POSITION.
WARNING
RX only. Administration of Nitrogen may be hazardous or contraindicated. For use only by or under the supervision of a licensed practitioner who is experienced in the use and administration of Nitrogen and is familiar with indications, effects, dosages, methods, and frequency and duration of administration, and with the hazards, contraindications and side effects, and the precautions to be taken.
WARNING
CONTAINS REFRIGERATED GAS; MAY CAUSE CRYOGENIC BURNS OR INJURY. MAY DISPLACE OXYGEN AND CAUSE RAPID SUFFOCATION.
Do not handle until all safety precautions have been read and understood. Use and store only outdoors or in a well-ventilated place. Wear cold insulating gloves, face shield, and eye protection. Use a back flow preventive device in the piping. DO NOT change or force fit connections. Close valve after each use and when empty. Always keep containers in upright position.
READ AND FOLLOW THE SAFETY DATA SHEET (SDS) BEFORE USE.
CAS: 77227-37-9
FIRST AID
IF INHALED: Remove person to fresh air and keep comfortable for breathing.
IF ON SKIN: Thaw frosted parts with lukewarm water. Do not rub affected area. Get immediate medical advice/attention.
PURITY CYLINDER GASES, INC.
2580 28TH ST SW, WYOMING, MI 49519
616-532-2375
DO NOT REMOVE THIS PRODUCT LABEL liquid nitrogenliquid nitrogen

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
311998nitrogen 99 % Gas for InhalationPSN12
311998nitrogen 99 % Gas for InhalationSCD12

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10927-106-01NITROGEN10 L in 1 DEWARLIQUID1012
10927-106-02NITROGEN20 L in 1 DEWARLIQUID2012
10927-106-03NITROGEN30 L in 1 DEWARLIQUID3012
10927-106-04NITROGEN40 L in 1 DEWARLIQUID4012
10927-106-06NITROGEN200 L in 1 DEWARLIQUID20012
10927-106-07NITROGEN50 L in 1 DEWARLIQUID5012
10927-106-08NITROGEN180 L in 1 DEWARLIQUID18012
10927-106-09NITROGEN230 L in 1 DEWARLIQUID23012

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10927-106NITROGEN LIQUID [PURITY CYLINDER GASES INC]12Legacy NDC, 8 package rows20181101_7b54ad8c-d5b2-435b-b0aa-36d84e59e823.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
NITROGENACTIVE INGREDIENTN762921K755
NITROGENACTIVE MOIETYN762921K755

Products#

Every source-derived product name is available through these pages.

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NDC Codes#

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
NITROGENN762921K75ACTIB

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
798b009a-a0ea-b750-e053-2991aa0a97917b54ad8c-d5b2-435b-b0aa-36d84e59e8232018-10-31Exact identifier
spl id: 798b009a-a0ea-b750-e053-2991aa0a9791
spl set id: 7b54ad8c-d5b2-435b-b0aa-36d84e59e823

Reported adverse events (FAERS/openFDA)#

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