Profend Nasal Antiseptic Kit

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 Antiseptic Kit
Generic name: POVIDONE IODINE USP, 10% W/W
Manufacturer: Professional Disposables International, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 3eeddd1d-7190-b35c-e063-6394a90ae816
SPL ID: 4d4d5003-bf7f-046e-e063-6394a90a3fc6
Version: 2
Effective date: 2026-03-18
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 05:15:45

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.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		Profend Nasal Antiseptic Kit	openfda.brand_name
generic name		POVIDONE IODINE USP, 10% W/W	openfda.generic_name
manufacturer name		Professional Disposables International, Inc.	openfda.manufacturer_name
ndc	package	10819-3889-1	openfda.package_ndc
ndc	package	10819-3889-3	openfda.package_ndc
ndc	package	10819-3889-2	openfda.package_ndc
ndc	product	10819-3889	openfda.product_ndc
ndc11	package	10819388901	derived:openfda.package_ndc
ndc11	package	10819388902	derived:openfda.package_ndc
ndc11	package	10819388903	derived:openfda.package_ndc
rxcui		1037205	openfda.rxcui
spl id		4d4d5003-bf7f-046e-e063-6394a90a3fc6	id
spl set id		3eeddd1d-7190-b35c-e063-6394a90ae816	set_id
unii		85H0HZU99M	openfda.unii

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.