FDA label 7ef8eaf2-023c-4b99-a62a-daea2c0a8802

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
2a16263a-a33c-4ef5-b7bf-129d36a7eb88
SPL ID
7ef8eaf2-023c-4b99-a62a-daea2c0a8802
Version
3
Effective date
2024-03-06
Source export date
2026-10-12
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/2026-10-12/b939c18fdf51df171cf60ce5558819d08ac66bb16bb9991d48cbec91028d783e/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:36:55

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 ■ FOR EXTERNAL USE ONLY ■ If you experience any symptoms such as redness, swelling or itchiness during usage or from exposure to direct sunlight after usage, suspend use and consult a physician ■ Do not use on wounds or other areas of skin irritation ■ Keep out of reach of children ■ Keep away from direct sunlight

Reported adverse events (FAERS/openFDA)#

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