Nitrous Oxide
- Manufacturer
- General Air Service & Supply Co
- Effective date
- 2025-11-26
- Label type
- PRESCRIPTION ANIMAL DRUG LABEL
- Version
- 4
- Source
- full-release
- Hydrated at
- 2026-06-01 02:45:20
Label at a glance#
ProductNitrous Oxide
Active ingredientNITROUS OXIDE
Label structure1 sections
Contacts and useful links#
Label contents#
Full prescribing information#
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
NITROUS OXIDE,
REFRIGERATED LIQUID USP UN1070
NON-FLAMMABLE GAS 2 OXIDIZER 5.1
34500DL (04/15)
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, effective 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 CRYOGENIC 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 value after each use and when empty. 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 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
FILLED and INSPECTED BY
GENERAL AIR SERVICE and SUPPLY
1105 ZUNI ST. DENVER, CO 80204. 303-892-7003
DailyMed RxNorm Mappings#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 21220-022-01 | Nitrous Oxide | 160 L in 1 DEWAR | GAS | 160 | 4 | |
| 21220-022-02 | Nitrous Oxide | 196 L in 1 DEWAR | GAS | 196 | 4 | |
| 21220-022-03 | Nitrous Oxide | 13818 L in 1 CYLINDER | GAS | 13818 | 4 | |
| 21220-022-04 | Nitrous Oxide | 7391 L in 1 CYLINDER | GAS | 7391 | 4 | |
| 21220-022-05 | Nitrous Oxide | 1642 L in 1 CYLINDER | GAS | 1642 | 4 | |
| 21220-022-06 | Nitrous Oxide | 765 L in 1 CYLINDER | GAS | 765 | 4 |
Products#
Every source-derived product name is available through these pages.
- Nitrous Oxide
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 21220-022 | 21220-022-01, 21220-022-02, 21220-022-03, 21220-022-04, 21220-022-05, 21220-022-06 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| NITROUS OXIDE | K50XQU1029 | ACTIB |
Source Document#
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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.