FDA label 7d84b946-1881-41d9-a3f3-9c67e98b69e4

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)

SPL set ID
6af1d0e6-bf6a-496c-9234-09ae1dd1aaa0
SPL ID
7d84b946-1881-41d9-a3f3-9c67e98b69e4
Version
2
Effective date
2010-01-01
Source export date
2026-10-12
Source partition
9
Source file
https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/fb14b8f3d34b45230a84f851c029385f512adf3f002423a9b78d4f7ca626ecec/drug-label-0009-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:22:30

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 KEEP ALL OIL, GREASE, AND HYDROCARBONS AWAY. USE ONLY WITH EQUIPMENT DESIGNED AND CLEANED FOR OXYGEN SERVICE AND RATED FOR CYLINDER PRESSURE. OPEN VALVE SLOWLY AND CLOSE AFTER EACH USE. ALWAYS SECURE CYLINDER. STORE AND USE WITH ADEQUATE VENTILATION. USE A BACK FLOW PREVENTATIVE DEVICE IN THE PIPING. CYLINDER TEMPERATURE SHOULD NOT EXCEED 52 DEGREES C (125 DEGREES F) USE IN ACCORDANCE WITH RWS MSDS-OXY. WARNING: FOR EMERGENCY USE ONLY WHEN ADMINISTERED BY PROPERLY TRAINED PERSONNEL FOR OXYGEN DEFICIENCY AND RESUSCITATION. FOR ALL OTHER MEDICAL APPLICATIONS Rx ONLY. WARNING: 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 ATTEMPT TO USE ON PATIENTS WHO HAVE STOPPED BREATHING UNLESS USED IN CONJUNCTION WITH RESUSCITATIVE EQUIPMENT. DO NOT REMOVE THIS PRODUCT LABEL.

Reported adverse events (FAERS/openFDA)#

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