FDA.reportPublic FDA data

FDA label 9f1e9e02-0df7-4a05-8140-892c6ec00a02

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
92af8b60-b612-4484-9830-e399bee6e6c4
SPL ID
9f1e9e02-0df7-4a05-8140-892c6ec00a02
Version
1
Effective date
2018-06-25
Source export date
2026-08-01
Source partition
2
Source file
https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-08-01/5cbbf4af8f4e275ec50931155b30ffa7322568b9af8a1c936a47f6d6774862fd/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:03:12

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. Do not use on: deep or puncture wounds, animal bites, serious burns When using this product: use only as directed, avoid contact with eyes or mucous membrane Stop use and ask a doctor if: Redness occurs, irritation develops, symptoms persist for more than 7 days, or clear up and occur again within a few days If pregnant or breast-feeding ask a health professional before use.