FDA.reportPublic FDA data

FDA label dda392fc-cc80-4210-a009-da746d178917

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
aabc9a44-e50e-40df-ae73-ab93537e63c9
SPL ID
dda392fc-cc80-4210-a009-da746d178917
Version
4
Effective date
2026-05-15
Source export date
2026-09-28
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/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:27:15

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 2 matching rows.

warnings

Warnings For external use only . When using this product avoid contact with the eyes. Stop use and ask a doctor if condition worsens or does not improve after 7 days. Ke ep out of the reach of children to prevent accidental ingestion. If swallowed, seek medical help or call Poison Control Center (1-800-222-1222) immediately.

warnings

Warnings For external use only . When using this product avoid contact with the eyes. Stop use and ask a doctor if condition worsens or does not improve after 7 days. Ke ep out of the reach of children to prevent accidental ingestion. If swallowed, seek medical help or call Poison Control Center (1-800-222-1222) immediately.

Reported adverse events (FAERS/openFDA)#

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