FDA label 32e11d95-6d10-5f95-e063-6394a90aa796

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
1cb8b7d8-ae49-4923-ae26-9264db8cc9f9
SPL ID
32e11d95-6d10-5f95-e063-6394a90aa796
Version
2
Effective date
2025-04-16
Source export date
2026-10-12
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:29:56

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 and PRECAUTIONS: Keep out of reach of children.For external use only.Avoid contact with eyes ormucous membranes.Perform a patch test before firstuse. lf irritation occurs,discontinue use.May increase sun sensitivityuse SPF.

Reported adverse events (FAERS/openFDA)#

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