FDA label e4ea9a49-bf4d-bee5-e053-2a95a90a023d

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
e4ea9db9-aaba-fc7f-e053-2a95a90aaa2f
SPL ID
e4ea9a49-bf4d-bee5-e053-2a95a90a023d
Version
2
Effective date
2022-07-27
Source export date
2026-10-12
Source partition
13
Source file
https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/b8dac220ac9fc8ffb4d86c6e00ece30169fc4575ca0cc92e5c9ce1a524fb0249/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 03:05:18

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. 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 the 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.