Nitrous Oxide
- Manufacturer
- Airtec Gases, LLC
- Effective date
- 2026-10-06
- Label type
- HUMAN PRESCRIPTION DRUG LABEL
- Version
- 12
- Source
- daily-update
- Hydrated at
- 2026-10-10 01:04:41
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
NITROUS OXIDE USP Label
NITROUS OXIDE USP
UN1070 Rx ONLY
NON-FLAMMABLE GAS 2 OXIDIZER 5.1
NET CONTENTS:
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; OXIDER, CONTAINS GAS UNDER PRESSURE; MAY EXPLODE IF HATED. MAY CAUSE DROWSINESS OR DIZZINESS; MAY DISPLACE OXYGEN AND CAUSE RAPID SUFFOCATION. MAY CAUSE FROSTBITE. Do not handle until all safety precautions have been read and understood. Keep valves and 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 flor preventative 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 52C (125F). 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 DO NOT REMOVE THIS PRODUCT LABEL.
DISTRIBUTED BY:
AIRTEC GASES
LAS VEGAS, NV 89109
(702) 454-2400
ATG-05 A15
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| NITROUS OXIDE | ACTIVE INGREDIENT | K50XQU1029 | 1 | |
| NITROUS OXIDE | ACTIVE MOIETY | K50XQU1029 | 1 |
Products#
Every source-derived product name is available through these pages.
- NITROUS OXIDE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 24312-003 | 24312-003-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| NITROUS OXIDE | K50XQU1029 | ACTIB |
Source Document#
Older Hydrated Versions#
| Version | Effective date | Source | Hydrated |
|---|---|---|---|
| 11 | 2025-10-13 | full-release | 2026-05-31 22:00:57 |
| 10 | 2024-10-04 | full-release | 2026-05-31 21:13:36 |
Orange Book application contexts#
All distinct exact application/product contexts derived from this label’s complete NDC list are paginated below.
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| NITROUS OXIDE | NITROUS OXIDE | Airtec Gases, LLC | 00d2e785-1cdc-496d-abd3-b255ae1cb693 | 2025-10-13 | 24312-003-01 24312-003 24312000301 00d2e785-1cdc-496d-abd3-b255ae1cb693 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
