FDA label 12f2c9c9-2801-42d2-aac7-34ab2b1f936d

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
2e1625cd-7337-4eed-95b1-b371c7169b97
SPL ID
12f2c9c9-2801-42d2-aac7-34ab2b1f936d
Version
2
Effective date
2018-02-20
Source export date
2026-10-12
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/2026-10-12/4760f38f2bcb10aa20ddbadb42b270d31e9f2a8024440d3af3dec8d11feb92ec/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:29:25

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

WARNING This package is intended for institutional use. KEEP THIS AND ALL DRUGS OUT OF THE REACH OF CHILDREN. This unit-dose package is not child-resistant. If dispensed for outpatient use, a child-resistant container should be utilized. To report a serious adverse event or obtain product information contact 1-800-343-9497.

Reported adverse events (FAERS/openFDA)#

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