OXYGEN

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: OXYGEN
Generic name: OXYGEN
Manufacturer: Bernens Convalescent Pharmacy, Inc
Product type: HUMAN PRESCRIPTION DRUG
SPL set ID: 239f2e15-2803-490c-bbf0-ce3c15a63705
SPL ID: 461867bf-019d-3b11-e063-6394a90a4ca3
Version: 9
Effective date: 2025-12-16
Source export date: 2026-09-28
Source partition: 2
Source file: https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:14:51

Harmonized routes table
Harmonized routes
RESPIRATORY (INHALATION)

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 22 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		OXYGEN	openfda.brand_name
generic name		OXYGEN	openfda.generic_name
manufacturer name		Bernens Convalescent Pharmacy, Inc	openfda.manufacturer_name
ndc	package	57957-0007-5	openfda.package_ndc
ndc	package	57957-0007-7	openfda.package_ndc
ndc	package	57957-0007-6	openfda.package_ndc
ndc	package	57957-0007-2	openfda.package_ndc
ndc	package	57957-0007-1	openfda.package_ndc
ndc	package	57957-0007-4	openfda.package_ndc
ndc	package	57957-0007-3	openfda.package_ndc
ndc	product	57957-0007	openfda.product_ndc
ndc11	package	57957000701	derived:openfda.package_ndc
ndc11	package	57957000703	derived:openfda.package_ndc
ndc11	package	57957000707	derived:openfda.package_ndc
ndc11	package	57957000706	derived:openfda.package_ndc
ndc11	package	57957000702	derived:openfda.package_ndc
ndc11	package	57957000704	derived:openfda.package_ndc
ndc11	package	57957000705	derived:openfda.package_ndc
rxcui		312172	openfda.rxcui
spl id		461867bf-019d-3b11-e063-6394a90a4ca3	id
spl set id		239f2e15-2803-490c-bbf0-ce3c15a63705	set_id
unii		S88TT14065	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings and cautions

PRODUCT WARNINGS AND PRECAUTIONS FIRST AID: FOR OXYGEN DEFICIENCY IN BREATHING PERSONS OR EMERGENCY RESUSCITATION WHEN USED BY PERSONNEL INSTRUCTED IN OXYGEN ADMINISTRATION. FOR OTHER MEDICAL APPLICATIONS USE ONLY AS DIRECTED BY A LICENSED PRACTITIONER. UNINTERRUPTED USE OF HIGH CONCENTRATIONS OF OXYGEN OVER A LONG DURATION WITHOUT MONITORING ITS EFFECT ON OXYGEN CONTENT OF ARTERIAL BLOOD MAY BE HARMFUL. USE ONLY WITH PRESSURE REDUCING EQUIPMENT AND APPARATUS DESIGNED FOR OXYGEN. DO NOT REMOVE THIS PRODUCT LABEL. CAUTION: FEDERAL LAW PROHIBITS DISPENSING WITHOUT A PRESCRIPTION. IN CASE OF FROSTBITE OBTAIN PROFESSIONAL MEDICAL TREATMENT IMMEDIATELY.

Reported adverse events (FAERS/openFDA)#

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