FDA.reportPublic FDA data

FDA label f8ab1161-ee22-e62a-e053-6394a90a35cb

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
f0520969-8f9b-e679-e053-2a95a90ac9ad
SPL ID
f8ab1161-ee22-e62a-e053-6394a90a35cb
Version
2
Effective date
2023-04-06
Source export date
2026-08-01
Source partition
11
Source file
https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-08-01/8ac060fefb6f4d67c41cc2c9e4330286ca93c48094c18386c11bf706a1d8bd34/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:27:27

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.In the process of using this product, if the application site has abnormal symptoms or side effects such as erythema, redness, swelling or itching due to direct light, seek medical advice and consult a professional doctor immediately. 2.Avoid using it on wounds. 3.Keep the product out of reach of children. 4.If it accidentally gets into the eyes, immediately wash and flush eyes with clean water. 5.This product may cause skin and body allergies or aggravate existing abnormal skin reactions (edema, inflammation, etc.). If you have experienced prior allergic reactions, consult a professional doctor or pharmacist before use.