FDA label 57d22531-726e-431a-b05c-2f9d61a7adc2

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
5ab00342-0b14-4d21-848a-c3ecccac4457
SPL ID
57d22531-726e-431a-b05c-2f9d61a7adc2
Version
1
Effective date
2010-01-01
Source export date
2026-10-12
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/ff22b88bd32e56cbc369af80345075227138a42b1b3ba9a84f038fd5493a7a47/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:05:51

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

GENERAL WARNINGS AND PRECAUTIONS WARNING: SECURE ALL CYLINDERS WHILE IN STORAGE AND IN USE. CAUTION: HIGH PRESSURE GAS CAN CAUSE RAPID SUFFOCATION. STORE AND USE WITH ADEQUATE VENTILATION. USE EQUIPMENT RATED FOR CYLINDER PRESSURE. CLOSE VALVE AFTER EACH USE AND WHEN EMPTY. USE IN ACCORDANCE WITH MATERIAL SAFETY DATA SHEET (MSDS). FIRST AID: IF INHALED REMOVE TO FRESH AIR. IF NOT BREATHING GIVE ARTIFICIAL RESPIRATION. IF BREATHING DIFFICULT GIVE OXYGEN. CALL A PHYSICIAN. DO NOT REMOVE THIS PRODUCT LABEL

Reported adverse events (FAERS/openFDA)#

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