Nitrogen

Manufacturer
FULLERTON WELDING SUPPLY
Effective date
2025-11-21
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
9
Source
full-release
Hydrated at
2026-05-31 21:46:57

Label at a glance#

ProductNitrogen
Active ingredientNITROGEN
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Certificate of Analysis

By Air-Liquefaction Process

Product: NITROGEN NF*

Manufacturing Plant: Pryor, OK

Address: Hwy 69A & 412 B

Pryor, OK 74361

Date / Time: 8/16/2018 9:43:00 AM

Lot Number: 037-08/16/2018/09:43

Delivery Unit # (Tanker / Railcar): 037

Quantity / Level / Prossure Gross: 31245 Tare: Net: LBS

*NF/EP applies only when used in a medical application or by medical customers properly registered with the FDA

Product delivered has been tested for indicated parameters and satisfies the contractually guaranteed purity specifications. Results are nominal values within statistical accuracy of analytical test methods.

This certificate does not add to or replace the warranty, limitations of liability or other provisions of the agreement between parties.

Requirement Test Method Specification Limit Result

Nitrogen Diff ≥ 99.999 percent ≥ 99.999 percent

Oxygen ** Delta F FAH0100 ≤ 5.00 ppm .68 ppm

Odor ** Organoleptic None None

Ppm = parts per million by volume ppb = parts per billion by volume

*Analysis on storage tank on periodic basis

**Analysis of each delivery unit

Released By:

Released via Electronic Signature: no handwritten signature required

(Signature)

Kevin N. Shue

(Printed Name)

QA-046US (08/17)

USJS0I00239193000 AutoLand TM nitrogennitrogen

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
311998nitrogen 99 % Gas for InhalationPSN9
311998nitrogen 99 % Gas for InhalationSCD9

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
42751-1074-1Nitrogen15 L in 1 DEWARGAS159
42751-1074-2Nitrogen10 L in 1 DEWARGAS109
42751-1074-3Nitrogen20 L in 1 DEWARGAS209
42751-1074-4Nitrogen30 L in 1 DEWARGAS309
42751-1074-5Nitrogen100 L in 1 DEWARGAS1009
42751-1074-6Nitrogen180 L in 1 DEWARGAS1809
42751-1074-7Nitrogen260 L in 1 DEWARGAS2609

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
42751-107442751-1074-1, 42751-1074-2, 42751-1074-3, 42751-1074-4, 42751-1074-5, 42751-1074-6, 42751-1074-7

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
NitrogenNITROGENFULLERTON WELDING SUPPLY74aa9180-1ea2-01fc-e053-2a91aa0aa6e12025-11-21Exact identifier
ndc (package): 42751-1074-2
ndc (package): 42751-1074-6
ndc (package): 42751-1074-4
ndc (package): 42751-1074-7
ndc (package): 42751-1074-1
ndc (package): 42751-1074-3
ndc (package): 42751-1074-5
ndc (product): 42751-1074
ndc11 (package): 42751107406
ndc11 (package): 42751107403
ndc11 (package): 42751107402
ndc11 (package): 42751107401
ndc11 (package): 42751107407
ndc11 (package): 42751107404
ndc11 (package): 42751107405
spl id: 4422eb42-3283-b410-e063-6394a90ae144
spl set id: 74aa9180-1ea2-01fc-e053-2a91aa0aa6e1

Reported adverse events (FAERS/openFDA)#

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