FDA label f2737da0-a8f2-ebf7-e053-2995a90aef2a

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
e7e8db77-1c0a-4313-9f53-24dca617a4db
SPL ID
f2737da0-a8f2-ebf7-e053-2995a90aef2a
Version
5
Effective date
2023-01-17
Source export date
2026-11-06
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/bbdc0a42bf44145a63c3752991067bece7e2a518be6cc14943d33c4987faa012/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:11:52

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

Warning: For external use only. Keep out of reach of children. Do not use in the eyes. Do not use on deep or puncture wounds, animal bites, or serious burns. Extended use may increase risk of sunburn. Stop use and ask doctor if condition worsens or symptoms last more than seven days.

Reported adverse events (FAERS/openFDA)#

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