FDA.reportPublic FDA data

FDA label 4a4be12b-d4df-c02f-e063-6294a90aea74

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
36068d1d-e2d0-22dd-e063-6394a90af427
SPL ID
4a4be12b-d4df-c02f-e063-6294a90aea74
Version
2
Effective date
2026-02-08
Source export date
2026-09-28
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:25:51

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

Warnings ·In case of having the same symptoms above on the part you put this product on by direct sunlight. ·You should avoid using this product under direct sunlight,especially on areas with scars, eczema, or dermatitis. ·In case of having following symptoms after using this,you're advised to stop using it immediately. If you keep using it,the symptoms will get worse and need to consult a dermatologist:In case of having problems such as red rash,swelling, itching,stimulation during usage.

warnings

Warnings ·In case of having the same symptoms above on the part you put this product on by direct sunlight. ·You should avoid using this product under direct sunlight,especially on areas with scars, eczema, or dermatitis. ·In case of having following symptoms after using this,you're advised to stop using it immediately. If you keep using it,the symptoms will get worse and need to consult a dermatologist:In case of having problems such as red rash,swelling, itching,stimulation during usage.

Reported adverse events (FAERS/openFDA)#

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