FDA.reportPublic FDA data

FDA label eae41917-929e-fbfa-e053-2995a90a9c52

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
eae41917-929d-fbfa-e053-2995a90a9c52
SPL ID
eae41917-929e-fbfa-e053-2995a90a9c52
Version
1
Effective date
2022-10-13
Source export date
2026-09-28
Source partition
1
Source file
https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/9c7783846d422acb0c9e59457606951c785a7d28cc631c8cc4839d0dc7c55f39/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:13:56

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 · Stop use and consult a specialist if there are any abnormal symptoms or side effects such as red spots, swelling or itching, due to direct sunlight when using or after using the product. · Do not use in areas with open wounds. · Keep out of reach of children. · When using the product, wash the eye immediately if it gets into the eye. · Do not leave the product unwashed, as it may cause hair loss or bleaching if it is not rinsed with water. · Keep it away from direct sunlight.

Reported adverse events (FAERS/openFDA)#

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