FDA label b41a96ef-a3f9-4cbe-be81-62109572af9c

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
4f23af51-8428-3d7d-e054-00144ff88e88
SPL ID
b41a96ef-a3f9-4cbe-be81-62109572af9c
Version
2
Effective date
2021-05-12
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 03:01:06

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

1) Consult with physician if you develop red, swollen or itchy skin or other abnormal or side effects during or after use owing to direct sunlight. 2) Limit the use on the open wounds. 3) Do not apply this product on the burned skin. 4) For external use only. 5) Avoid contact use eyes.

Reported adverse events (FAERS/openFDA)#

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