FDA label 3d68e9fd-e272-4905-983e-45675281b9e0

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
da68fdb7-2c02-4b28-aba3-b9bb6d203b72
SPL ID
3d68e9fd-e272-4905-983e-45675281b9e0
Version
1
Effective date
2011-05-02
Source export date
2026-11-06
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/bbdc0a42bf44145a63c3752991067bece7e2a518be6cc14943d33c4987faa012/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:10:01

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

FOR EXTERNAL USE ONLY. USE CARE DURING APPLICATION TO AVOID GETTING IN EYE. IF DISCOMFORT OR IRRITATIONDEVELOPS, WASH OFF GENTLY AND DISCONTINUE USE.

Reported adverse events (FAERS/openFDA)#

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