FDA label fe25b91e-4c24-07a1-e053-6394a90a20d9

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
ec12378e-00b0-4ca6-ae65-9f64f9f15a94
SPL ID
fe25b91e-4c24-07a1-e053-6394a90a20d9
Version
5
Effective date
2023-06-15
Source export date
2026-10-12
Source partition
12
Source file
https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/edd23646015c9adc800cdbe2b778398a2d2b70e90dce5721ef2b191499a0397f/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:59:08

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 •if you have ever had an allergic reaction to this product or any of its ingredients. Ask a doctor before use if you have •deep or puncture wounds •animal bites •serious burns. When using this product •do not use in or near eyes •do not apply over large areas of the body or in large quantities •do not apply over raw surfaces or blistered areas. Stop use and ask a doctor if •condition worsens •symptoms persist for more than 7 days, or clear up and occur again within a few days.

Reported adverse events (FAERS/openFDA)#

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