FDA label 180c6cf8-ac82-50c0-e063-6294a90ae391

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
bb5f6bb3-c20c-4326-9b8d-ac7f7d2f4274
SPL ID
180c6cf8-ac82-50c0-e063-6294a90ae391
Version
4
Effective date
2024-05-09
Source export date
2026-10-12
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/b939c18fdf51df171cf60ce5558819d08ac66bb16bb9991d48cbec91028d783e/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:38:37

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

WARNINGS FOR EXTERNAL USE ONLY: HANDS WHEN USING THIS PRODUCT KEEP OUT OF AND AWAY FROM EYES IN CASE OF CONTACT WITH EYES, FLUSH THOROUGHLY WITH WATER DO NOT INHALE OR INGEST STOP USE AND ASK DOCTOR IF IRRITATION OR REDNESS DEVELOPS CONDITION PERSISTS

Reported adverse events (FAERS/openFDA)#

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