FDA.reportPublic FDA data

NITROUS OXIDE

Manufacturer
Air Source Industries
Effective date
2024-10-06
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
14
Source
full-release
Hydrated at
2026-05-31 21:13:48

Label at a glance#

ProductNITROUS OXIDE
Active ingredientNITROUS OXIDE
Label structure1 sections

Label contents#

Full prescribing information#

NITROUS OXIDE COMPRESSED, USP LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NITROUS OXIDE USP UN1070

                                                DO NOT REMOVE THIS LABEL.

NON-FLAMMABLE GAS  2       34436 (05/18)                                     OXIDIZER 5.1    

Rx only. WARNING: Administration of Nitrous Oxide may be hazardous or contraindicated. For use only by or under supervision of a licensed practitioner who is experienced in the use and administration of Nitrous Oxide and is familiar with the indications, effects, dosages, methods, and frequency and duration of administration, and with the hazards, contraindications, and side effects and the precautions to be taken. DANGER: MAY CAUSE OR INTENSIFY FIRE, OXIDIZER. CONTAINS GAS UNDER PRESSURE; MAY EXPLODE IF HEATED. MAY CAUSE DROWSINESS OR DIZZINESS. MAY DISPLACE OXYGEN AND CAUSE RAPID SUFFOCATION. MAY CAUSE FROSTBITE. Do not handle until all safety precautions have been rad and understood. Keep and store away from clothing and other combustible materials. Keep valves ad fittings free from grease and oil. Avoid breathing gas. Do not get in eyes, on skin, or on clothing. 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 ambient temperature exceeds 52oC (125oF). Read and follow the Safety Data Sheet (SDS) before use. FIRST AID: IF INHALED: Remove person to fresh air and keep comfortable for breathing. Call a POISON CENTER or doctor/physician if you feel unwell. IF ON SKIN:  Thaw frosted parts with lukewarm water. Do not rub affected area. Get immediate medical advice/attention. CAS: 10024-97-2

WARNING: This product contains a chemicals including Nitrous Oxide, which is known to the state of California to cause birth defects or other reproductive harm. For more information go to www.p65warning.ca.gov

AIR SOURCE INDUSTRIES INC.

3976 CHERRY AVE • LONG BEACH, CA 90807

(562) 426-4017

Nitrous Oxide Shoulder LabelNitrous Oxide Shoulder Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
312022nitrous oxide 99 % Gas for InhalationPSN14
312022nitrous oxide 99 % Gas for InhalationSCD14

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10167-200-01NITROUS OXIDE368 L in 1 CYLINDERGAS36814
10167-200-02NITROUS OXIDE940 L in 1 CYLINDERGAS94014
10167-200-03NITROUS OXIDE1590 L in 1 CYLINDERGAS159014
10167-200-04NITROUS OXIDE1232 L in 1 CYLINDERGAS123214
10167-200-05NITROUS OXIDE7570 L in 1 CYLINDERGAS757014
10167-200-06NITROUS OXIDE12300 L in 1 CYLINDERGAS1230014
10167-200-07NITROUS OXIDE13800 L in 1 CYLINDERGAS1380014
10167-200-08NITROUS OXIDE4944 L in 1 CYLINDERGAS494414
10167-200-09NITROUS OXIDE2.25 L in 1 CYLINDERGAS2.2514
10167-200-10NITROUS OXIDE9 L in 1 CYLINDERGAS914
10167-200-11NITROUS OXIDE22.5 L in 1 CYLINDERGAS22.514

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10167-200NITROUS OXIDE GAS [AIR SOURCE INDUSTRIES]14Current NDC, Legacy NDC, 11 package rows20241008_eebd56c1-4ab3-409b-9767-e54dc42f2fce.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
NITROUS OXIDEACTIVE INGREDIENTK50XQU10293
NITROUS OXIDEACTIVE MOIETYK50XQU10293

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
10167-20010167-200-01, 10167-200-02, 10167-200-03, 10167-200-04, 10167-200-05, 10167-200-06, 10167-200-07, 10167-200-08, 10167-200-09, 10167-200-10, 10167-200-11

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
NITROUS OXIDEK50XQU1029ACTIB

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
NITROUS OXIDENITROUS OXIDEAir Source Industrieseebd56c1-4ab3-409b-9767-e54dc42f2fce2024-10-06Exact identifier
ndc (package): 10167-200-04
ndc (package): 10167-200-09
ndc (package): 10167-200-01
ndc (package): 10167-200-08
ndc (package): 10167-200-07
ndc (package): 10167-200-11
ndc (package): 10167-200-02
ndc (package): 10167-200-10
ndc (package): 10167-200-03
ndc (package): 10167-200-05
ndc (package): 10167-200-06
ndc (product): 10167-200
ndc11 (package): 10167020007
ndc11 (package): 10167020010
ndc11 (package): 10167020003
ndc11 (package): 10167020005
ndc11 (package): 10167020006
ndc11 (package): 10167020009
ndc11 (package): 10167020008
ndc11 (package): 10167020002
ndc11 (package): 10167020011
ndc11 (package): 10167020004
ndc11 (package): 10167020001
spl id: c86cf8bb-09c3-434a-8514-2353f4f43d68
spl set id: eebd56c1-4ab3-409b-9767-e54dc42f2fce

Reported adverse events (FAERS/openFDA)#

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