FDA label df6535ab-4484-4bc8-99c3-a8d0b5d1ffc8

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
6ab9fa6c-c95e-4c09-b306-00363eb244de
SPL ID
df6535ab-4484-4bc8-99c3-a8d0b5d1ffc8
Version
3
Effective date
2012-03-28
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 05:12:54

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

WARNING Do not apply to fresh arterial clots. Avoid contact with eyes. Keep this and all medications out of the reach of children. In case of accidental overdose seek professional assistance or contact a Poison Control Center immediately. Use only as directed. When applied to a sensitive area, a temporary stinging sensation may be noted.

Reported adverse events (FAERS/openFDA)#

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