FDA label 458cc057-fb93-4aa4-adc1-7c016c9b38d5

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
c3da38ad-199e-436d-9374-afd1da36c473
SPL ID
458cc057-fb93-4aa4-adc1-7c016c9b38d5
Version
1
Effective date
2021-09-13
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 07:05:32

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. ​Do not use on wounds or damage skin. When using this product :​ avoid bandaging tightly, aviod contact with eyes, ​keep out of mreach of childern ​. ​Stop use and ask doctor if : ​ condition worsens, symptoms persist for more than 7 days, clear up and within a few days.

Reported adverse events (FAERS/openFDA)#

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