Nitrous Oxide
- Manufacturer
- AGL Welding Supply Co., Inc.
- Effective date
- 2026-01-01
- Label type
- HUMAN PRESCRIPTION DRUG LABEL
- Version
- 13
- Source
- full-release
- Hydrated at
- 2026-05-31 22:06:31
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Nitrous Oxide, Refrigerated Liquid USP UN2201 NON-FLAMMABLE GAS 2 OXIDIZER 5.1
AGL Certified ISO 9001:2008 Inhalation Therapy Co. 973-478-5100 600 RT. 46 WEST, CLIFTON, NJ 07015
ALWAYS KEEP CONAINER IN UPRIGHT POSITION
WARNING: Rx only. 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, contraindications and side effects, and the precautions to be taken. DANGER: MAY CAUSE OR INTENSIFY FIRE; OXIDIZER CONTAINS REFRIGERATED GAS; MAY CAUSE CRYOGENIC BURNS OR INJURY. MAY CAUSE DROWSINESS OR DIZZINESS. MAY DISPLACE OXYGEN AND CAUSE RAPID SUFFOCATION. Do not handle until all safety precautions have been read and understood. Keep and store away from clothing and other combustible materials. Keep valves and fittings free from grease and oil. Avoid breathing gas. Use and store only outdoors or in a well-ventilated place. Wear cold insulating gloves, face shield, and eye protection. 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. Avoid spills. Do not walk on or roll equipment over spills. Close valve after each use and when empty. Read and follow the Safety Data Sheet (SDS) before use. FIRST AID 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 LABEL.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
NITROUS OXIDE, USP UN1070 NON-FLAMMABLE GAS 2 OXIDIZER 5.1
Rx only. 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, contraindications and side effects, and the precautions to be taken. DANGER: MAY CAUSE OR INTENSIFY FIRE; OXIDIZER CONTAINS GAS UNDER PESSURE; 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 read and understood. Keep and store away from clothing and other combustible materials. Keep valves and fittings free from grease and oil. Avoid breathing gas. Do not put 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 52 degrees C (125 degrees F). 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 LABEL. Size: E Liters: 1,478 E
AGL Certified ISO 9001:2008 Inhalation Therapy Co. 600 RT. 46 WEST, CLIFTON, NJ 07015 973-478-5100
DailyMed RxNorm Mappings#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 17575-011-01 | Nitrous Oxide | 12320 L in 1 CYLINDER | GAS | 12320 | 13 | |
| 17575-011-02 | Nitrous Oxide | 4928 L in 1 CYLINDER | GAS | 4928 | 13 | |
| 17575-011-03 | Nitrous Oxide | 3696 L in 1 CYLINDER | GAS | 3696 | 13 | |
| 17575-011-04 | Nitrous Oxide | 2464 L in 1 CYLINDER | GAS | 2464 | 13 | |
| 17575-011-05 | Nitrous Oxide | 1478 L in 1 CYLINDER | GAS | 1478 | 13 | |
| 17575-011-06 | Nitrous Oxide | 99792 L in 1 CYLINDER | GAS | 99792 | 13 |
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 |
|---|---|
| 17575-011 | 17575-011-01, 17575-011-02, 17575-011-03, 17575-011-04, 17575-011-05, 17575-011-06 |
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 | 2023-10-06 | full-release | 2026-05-31 20:53:46 |
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 | AGL Welding Supply Co., Inc. | 75c1da96-5cc4-4826-bbd0-dc6a9142b51c | 2026-01-01 | 17575-011-03 17575-011-05 17575-011-01 17575-011-06 17575-011-04 17575-011-02 17575-011 17575001106 17575001102 17575001103 17575001105 17575001101 17575001104 41c35885-084f-fead-e063-6394a90a98db 75c1da96-5cc4-4826-bbd0-dc6a9142b51c |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.

