Nitrous Oxide

Manufacturer
Inland Welding Supply dba A-L Compressed Gases | A-L Compressed Gases
Effective date
2010-02-12
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:52:51

Label at a glance#

ProductNitrous Oxide
Active ingredientNitrous Oxide
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NITROUS OXIDE
USP
UN 1070     RX ONLY

WARNING: DO NOT HANDLE CYLINDER OR USE CONTENTS UNTIL 1) YOU HAVE READ AND UNDERSTAND THE MATERIAL SAFETY DATA SHEET FOR THIS PRODUCT.  CALL 1-800-231-1366 FOR MORE COPIES.        2) YOU ARE TRAINED TO USE CYLINDER AND CONTENTS, INCLUDING EMERGENCY PROCEDURES.

NON-FLAMMABLE     2
OXIDIZER     5.1
 
WARNING: HIGH PRESSURE, OXIDIZING LIQUID AND GAS. VIGOROUSLY ACCELERATES 
COMBUSTION. CAN CAUSE RAPID SUFFOCATION AND DEATH WITHOUT WARNING (DUE T0
OXYGEN DEFICIENCY). CAN CAUSE ANESTHETIC EFFECTS. MAY CAUSE FROSTBITE. MAY
CAUSE NERVOUS SYSTEM INJURY AND EMBRYO FETAL TOXICITY. Avoid breathing gas. Secure cylinder and provide adequate ventilation in storage and use. Keep oil and grease away. No smoking in cylinder area. Do not use or store near heat or open flame. Use only with equipment cleaned for oxygen service and rated for cylinder pressure. Do not get liquid in eyes, on skin or clothing. Cylinder temperature should not exceed 125 degrees F (52 degrees C). Open valve slowly. Close valve after each use and when empty. Return with at least 25 PSIG pressure. Use in accordance with Material Safety Data Sheet. NOTE: Suck-back into cylinder may cause rupture. Always use a back-flow preventive device in the piping.
FIRST AID: IF INHALED, remove to fresh air. If not breathing, give artificial respiration. If breathing is difficult, give oxygen. Call a physician. IN CASE OF FROSTBITE, obtain medical treatment immediately.
WARNING: Administration of Nitrous Oxide 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 Nitrous Oxide and is familiar with the indications, effects, dosages, methods and frequency and duration of administration and with the hazards, contraindicated and side effects and the precautions to be taken. CAUTION: Federal law prohibits dispensing without prescription.

CAUTION: USE NO OIL ON VALVE OR CONNECTIONS. TRANSFILLING OF THIS GAS IS PROHIBITED.
DO NOT REMOVE THIS PRODUCT LABEL

A-L COMPRESSED GASES, INC.
4230 E. TRENT AVE.
SPOKANE, WA 99202

AL-M51-2            G05nitrous oxide labelnitrous oxide label

FDA-Initiated Inactive NDC Indexing#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
18482-128NITROUS OXIDE (NITROUX OXIDE) GAS [INLAND WELDING SUPPLY DBA A-L COMPRESSED GASES]1Legacy NDC20100719_d5c909b5-cddd-472c-b9a2-9463cfa67005.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
Nitrous OxideACTIVE INGREDIENTK50XQU10291
Nitrous OxideACTIVE MOIETYK50XQU10291

Products#

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

DailyMed product names page 1 of 1 · 2 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
18482-12818482-128-01, 18482-128-02, 18482-128-03, 18482-128-04

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 · Source PDF

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
2c51de9b-69a8-95f2-e063-6394a90a430bd5c909b5-cddd-472c-b9a2-9463cfa670052025-01-22Exact identifier
spl set id: d5c909b5-cddd-472c-b9a2-9463cfa67005

Reported adverse events (FAERS/openFDA)#

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