FDA label fb724322-dd19-4ebe-ae5b-aaed3b0ef111

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
0ec9a8b2-8792-4bbf-b4dc-992d8dadf217
SPL ID
fb724322-dd19-4ebe-ae5b-aaed3b0ef111
Version
5
Effective date
2013-05-03
Source export date
2026-09-28
Source partition
6
Source file
https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:39:46

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: Avoid contact with eyes. If contact occurs, rinse thoroughly with water. Discontinue use if signs of skin irritation develop or increase. If irritation persists, consult a health care practitioner. If swallowed, get medical help or contact a Poison Control Center right away. For external use only. Keep out of reach or children.

Reported adverse events (FAERS/openFDA)#

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