FDA label 95beb730-ec50-4fea-bd4b-146437b7092e

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
34501fd2-1c36-40a0-ba59-ebdbf4cb31d9
SPL ID
95beb730-ec50-4fea-bd4b-146437b7092e
Version
1
Effective date
2014-08-12
Source export date
2026-11-06
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/2026-11-06/d05434af5edc4383b7c7894a8f2d94df21171d17714450933cecdfc35cedfa3d/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 06:44:49

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

CAUTIONS: DO NOT USE THIS PRODUCT IF YOU HAVE A SENSITIVE SKIN. DO NOT APPLY TO THE WOUNDED OR DAMAGED SKIN. AVOID EYE CONTACT. DISCONTINUE USE IF SIGNS OF IRRITATION APPEAR. IF IRRITATION PERSISTS, CONSULT A DOCTOR. IF YOU ARE ALLERGIC TO ANY INGREDIENT IN THE PRODUCT, DO NOT USE.

Reported adverse events (FAERS/openFDA)#

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