FDA label 4833f8fa-f0bc-dd53-e063-6294a90a3899

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
9d237fb7-4f5f-521d-e053-2a95a90a9734
SPL ID
4833f8fa-f0bc-dd53-e063-6294a90a3899
Version
7
Effective date
2026-01-12
Source export date
2026-11-06
Source partition
14
Source file
https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/2cac198adf50bf0f7077ca012f418bbee1fb171f907f83d6a83048d9770d345b/drug-label-0014-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 08:12:19

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 • When using this product • Keep out of eyes. Rinse with water to remove • Stop use and ask doctor if • Rash or irritation occurs • Do not use • On damaged or broken skin • If allergic to any ingredient • If swallowed, get medical help or contact a Poison Control Center

Reported adverse events (FAERS/openFDA)#

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