FDA.reportPublic FDA data

FDA label 2cdece26-8bf9-478a-bc37-53bf699c9952

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
e0ac4390-4fad-466f-9f96-c1a499d37cef
SPL ID
2cdece26-8bf9-478a-bc37-53bf699c9952
Version
4
Effective date
2023-04-14
Source export date
2026-09-28
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:52:30

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: • Reuse of the product increases risk of infection. • Dispose carefully in a manner preventing cross-contamination. • For external use only. • Do not make reverse turns while wrapping Unnaplast ® bandage. • Do not use if you are hypersensitive to the product or any of its components. • Do not use on grossly macerated skin. • If condition worsens or does not improve within 7 days, consult a doctor. • Avoid contact with eyes. • Keep out of reach of children.

Reported adverse events (FAERS/openFDA)#

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