FDA label 59f2a203-8df6-46df-8a8c-c7e59e3c9ba2

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
ade67b24-9118-4c61-9924-97ad54e8f373
SPL ID
59f2a203-8df6-46df-8a8c-c7e59e3c9ba2
Version
2
Effective date
2016-06-23
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 03:01:52

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 2 matching rows.

warnings and cautions

​Warnings: Do not use on wounds, swollen areas or rashes. If your skin itches, reddens or becomes sensitive, discontinue use and contact a physician. Do not return product back into container once dispensed. If product come in contact with eyes, wash eyes immediately with water. Store in a cool, dry place and away from direct sunlight. ​Keep out of reach of children.

warnings and cautions

Warnings: If product come in contact with eyes, rinse well with water. Discontinue use if signs of irritation develop. Keep out of reach of children.

Reported adverse events (FAERS/openFDA)#

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