NITROUS OXIDE

Manufacturer: Badger Welding Supplies, Inc.
Effective date: 2026-02-12
Label type: HUMAN PRESCRIPTION DRUG LABEL
Version: 18
Source: full-release
Hydrated at: 2026-05-31 22:05:50

Label at a glance#

ProductNITROUS OXIDE

Active ingredientNITROUS OXIDE

Label structure1 sections

Contacts and useful links#

PhoneLabel contact608-257-5606

Label contents#

Full prescribing information#

NITROUS OXIDE USP LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NITROUS OXIDE USP

UN1070

NON-FLAMMABLE GAS 2

OXIDIZER 5.1

37736 (0317)

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 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 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 get in eyes, on skin or on clothing. Use an store only outdoors or in a well ventillated place. In case of fire: Stop leak if safe to do so. Use a back flow preventive device in the piping. Use only 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°C (125°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 frozen parts with lukewarm water. Do not rub affected area. Get immediate medical advice.attention. WARNING:This product contains a chemical known to the state of Califorina to cause birth defects or other reproductive harm. CAS: 10024-97-2

BADGER WELDING SUPPLIES, INC.

101 SOUTH DICKINSON STREET • MADISON WI 53704

608-257-5606

DO NOT REMOVE THIS LABEL

CONTENTS ________________________ LTRS. ____________________________________CU. FT.

Badger N2O2 SL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
312022	nitrous oxide 99 % Gas for Inhalation	PSN	18
312022	nitrous oxide 99 % Gas for Inhalation	SCD	18

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
12121-002-03	NITROUS OXIDE	4920 L in 1 CYLINDER	GAS	4920	18
12121-002-04	NITROUS OXIDE	7447 L in 1 CYLINDER	GAS	7447	18
12121-002-05	NITROUS OXIDE	13800 L in 1 CYLINDER	GAS	13800	18
12121-002-06	NITROUS OXIDE	1590 L in 1 CYLINDER	GAS	1590	18
12121-002-07	NITROUS OXIDE	215 L in 1 CYLINDER	GAS	215	18
12121-002-08	NITROUS OXIDE	632 L in 1 CYLINDER	GAS	632	18

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version	Uploaded
NITROUS OXIDE	ACTIVE INGREDIENT	K50XQU1029	2
NITROUS OXIDE	ACTIVE MOIETY	K50XQU1029	2

Products#

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NITROUS OXIDE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
12121-002	12121-002-06, 12121-002-03, 12121-002-04, 12121-002-05, 12121-002-07, 12121-002-08

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
Name	UNII	Kind
NITROUS OXIDE	K50XQU1029	ACTIB

Source Document#

Source XML

Orange Book application contexts#

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openFDA label cross-check#

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Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
NITROUS OXIDE	NITROUS OXIDE	Badger Welding Supplies, Inc.	45c57025-ae3a-4d36-b74f-83d39cf00b08	2026-02-12		Exact identifier ndc (package): 12121-002-06 ndc (package): 12121-002-03 ndc (package): 12121-002-04 ndc (package): 12121-002-05 ndc (package): 12121-002-08 ndc (package): 12121-002-07 ndc (product): 12121-002 ndc11 (package): 12121000203 ndc11 (package): 12121000207 ndc11 (package): 12121000206 ndc11 (package): 12121000208 ndc11 (package): 12121000205 ndc11 (package): 12121000204 spl id: 4aa5a28e-aba7-2354-e063-6394a90af99e spl set id: 45c57025-ae3a-4d36-b74f-83d39cf00b08

Reported adverse events (FAERS/openFDA)#

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