FDA label 56fe6b3f-b054-4c84-9d18-b28d361e1cd4

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
0277f48f-02aa-482c-9e9e-e2aa8d7317f6
SPL ID
56fe6b3f-b054-4c84-9d18-b28d361e1cd4
Version
2
Effective date
2017-01-20
Source export date
2026-11-06
Source partition
13
Source file
https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/245ea1c0d730b312e4410f082201cbe2cb4d1936fa2918316b6ea631293cbeba/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 08:05:46

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 For external use only . Avoid contact with eyes. Stop use and ask a doctor if •increased skin irritation or other allergic reaction develops. •symptoms worsen or do not improve within 7 days. Nursing mothers should not apply to bre ast area . Keep out of reach of children. If swallowed , get medical help or contact a Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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