FDA label 595e3b62-56b5-4a6d-b030-cdf1f3a5c15f

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
289b5922-a65e-4256-b819-283ba3957c52
SPL ID
595e3b62-56b5-4a6d-b030-cdf1f3a5c15f
Version
1
Effective date
2017-12-06
Source export date
2026-10-12
Source partition
3
Source file
https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/f40eac55ff4c5d55c3d8bbc5766ea7e21e4196960cfb4703b96a406b491c0cd5/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:34:24

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 Warnings: 1. If there are any abnormal symptoms such as red spots, swelling, itching or side effects caused by direct sunlight, please consulting a specialist. 2. Do not user for wounded areas. 3. Storage and handling precautions. -Keep it out of the reach of children. -Keep away from direct sunlight. 4. Do not use for children under 3 years old. 5. Do not use during pregnancy. Do not use around the vulva after and before delivery.

Reported adverse events (FAERS/openFDA)#

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