Home FDA labels 40312dd9-3553-cdfb-e063-6394a90a3638 Profend Nasal Decolonization 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)
Brand name Profend Nasal Decolonization
Generic name POVIDONE IODINE USP, 10% W/W
Manufacturer Professional Disposables International, Inc.
Product type HUMAN OTC DRUG
SPL set ID 6245b1e5-6637-18bc-e053-2a91aa0aa981
SPL ID 40312dd9-3553-cdfb-e063-6394a90a3638
Version 12
Effective date 2025-10-02
Source export date 2026-09-28
Source partition 2
Source file https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 05:14:44 Harmonized routes table Harmonized routes TOPICAL
Harmonized identifier links# Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
Harmonized identifiers page 1 of 1 · 15 matching rows.
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 in the eyes or mouth on individuals who are allergic or sensitive to iodine over large areas of the body Stop use and ask doctor if irritation and redness develop or if condition persists for more than 72 hours. Ask a doctor before use if you have Deep or puncture wounds animal bites serious burns
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.