FDA label 547c05b8-ed93-4e8c-9124-66104f8ead97

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
5d8ad80b-9b66-440a-a499-624437f55ec5
SPL ID
547c05b8-ed93-4e8c-9124-66104f8ead97
Version
2
Effective date
2016-02-02
Source export date
2026-09-28
Source partition
11
Source file
https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:20:15

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 Avoid contact with eyes Do not use in large quantities, particularly over raw surfaces or blistered areas Stop use and ask a doctor if • Condition worsens, or if symptoms persist for more than 7 days or clear up and occur again with a few days. Discontinue use.

Reported adverse events (FAERS/openFDA)#

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