FDA label 24e2da13-4674-1757-e063-6394a90a3a6b

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
24e2da13-4673-1757-e063-6394a90a3a6b
SPL ID
24e2da13-4674-1757-e063-6394a90a3a6b
Version
138
Effective date
2024-10-20
Source export date
2026-11-06
Source partition
11
Source file
https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/2233cb6af8c6b55a5e4a05449e8db0d2f259f3c061d5d001b654a8bea1cc1db2/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:52:57

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: For external use only. Avoid contact with eyes. In case of accidental contact, rinse thoroughly with plenty of water. Discontinue use immediately if redness, itching, or any discomfort occurs. Do not use on broken, inflamed, or sensitive skin. Pregnant or nursing women should consult a doctor before use.

Reported adverse events (FAERS/openFDA)#

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