FDA.reportPublic FDA data

FDA label ffb65db9-5fa8-f891-e053-6394a90a83c2

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
a0c4a908-bf11-3886-e053-2995a90aafd1
SPL ID
ffb65db9-5fa8-f891-e053-6394a90a83c2
Version
3
Effective date
2023-07-04
Source export date
2026-09-28
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:52:31

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: For external use only: hands Flammable, keep away from fire or flame. When using this product: • Keep out of eyes. In case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin. • Do not inhale or ingest. • Use with caution if allergic. Stop use and ask a doctor if: • Irritation or redness develops. • Condition persists for more than 72 hours. Keep out of reach of children: If swallowed, get medical help right away. 50 ml label 500 ml label

Reported adverse events (FAERS/openFDA)#

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