FDA label 78357755-2560-1030-e053-2991aa0aaa04

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
78357755-255f-1030-e053-2991aa0aaa04
SPL ID
78357755-2560-1030-e053-2991aa0aaa04
Version
1
Effective date
2018-10-14
Source export date
2026-11-06
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/b00a73f24c6ff050408c570063640e3d80d1f71dfc9a165d1cf072a25659445a/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 06:59:54

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

For external use only. Do Not Use for arthritis-like conditions in children under 2. on wounds, damaged, broken or irritated skin When Using This Product use only as directed. do not bandage tightly. avoid contact with eyes or mucous membranes. Stop And Ask Doctor If condition worsens symptoms last more than 7 days symptoms clear up and com back in a few days Keep out of reach of children. If swalled get medical help or contact a Poison Control Center right away. If pregnant or breast-feeding , ask a health professional before use.

Reported adverse events (FAERS/openFDA)#

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