FDA label ebb7d481-2404-4b77-8d19-d9b2a9e8804f

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
10fef6ba-297f-4e5f-8769-d12ba94cdcba
SPL ID
ebb7d481-2404-4b77-8d19-d9b2a9e8804f
Version
2
Effective date
2024-08-21
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 01:27:32

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 Keep out of reach of children. For external use only. If swallowed, immediately call Poison Control 800-222-1222 Avoid contact with the eyes. Do not use in large quantities, particularly over raw skin surfaces or blistered areas. if you are allergic to any ingredient in this product. if you have an injury or perforation (hole) of the eardrum, including tubes in the ear. If conditions worsen, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a doctor.

Reported adverse events (FAERS/openFDA)#

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