FDA.reportPublic FDA data

FDA label cb9003ba-d188-4e2b-a716-f8acd2648b32

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
ad87d4f8-e195-40a8-b17b-36e8e5817719
SPL ID
cb9003ba-d188-4e2b-a716-f8acd2648b32
Version
2
Effective date
2018-11-28
Source export date
2026-10-12
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/2026-10-12/7928c8e8c6256620071a8b7e5b93eb8dfa543649c08d17a01ea02251012ba58c/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:26:30

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. Stop use if the following symptoms appear, continued use can worsen the situation. And please visit a doctor. - Red spot, swelling, itching generate when using it. - Above symptoms generates on applied area causing by UV. 2. Avoid applying to wound area, eczema, skin disease and so on. 3. Cautions for usage and storage - Please cover the cap after use. - Keep it out of reach of children. - Keep it store in shadow and avoid heat and cold place to store.

Reported adverse events (FAERS/openFDA)#

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