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

Warnings cross-check#

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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.