FDA.reportPublic FDA data

FDA label 09d6ad4d-5f98-559a-e063-6394a90a7f59

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
c46d15b0-9640-4aa1-a05a-e0bfe200e631
SPL ID
09d6ad4d-5f98-559a-e063-6394a90a7f59
Version
2
Effective date
2023-11-10
Source export date
2026-11-06
Source partition
13
Source file
https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/2d7d9682bb1dc608c198b25f4655629e874bd36827b741e40512d5288afcc775/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
8dff71fbef1291eb7711013e9a3a06194930757924a8946ae3034107a98d9463
Import run
20261106T075659Z
Imported at
2026-11-06 09:22:54

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 Keep out of 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 Keep out of 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.