FDA.reportPublic FDA data

FDA label b7676b00-faaf-41c5-bf78-ebe22d79a552

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
73e6213b-ab1e-4493-99bf-286197e1e0ec
SPL ID
b7676b00-faaf-41c5-bf78-ebe22d79a552
Version
1
Effective date
2012-11-29
Source export date
2026-08-01
Source partition
1
Source file
https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-08-01/0689a4374f1490600b5244071db3b04bd3bbc29ceda7a856edb8225323adf20a/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:00:18

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. 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 dematologists. 2. In case of having problems such as red spots, swelling, itching and irritation during usage 3. In case the above symptoms emerge due to direct exposure to sunlight 4. Please do not apply the skin to areas affected by eczema and dermatitis