Povidone-Iodine Gel

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: Povidone-Iodine Gel
Generic name: POVIDONE-IODINE
Manufacturer: Dukal LLC
Product type: HUMAN OTC DRUG
SPL set ID: 2bebe082-59b6-17c1-e063-6294a90a9a52
SPL ID: 43f8fa10-9266-a4f3-e063-6394a90a9e93
Version: 2
Effective date: 2025-11-19
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 05:54:28

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 · 10 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		Povidone-Iodine Gel	openfda.brand_name
generic name		POVIDONE-IODINE	openfda.generic_name
manufacturer name		Dukal LLC	openfda.manufacturer_name
ndc	package	65517-0070-1	openfda.package_ndc
ndc	product	65517-0070	openfda.product_ndc
ndc11	package	65517007001	derived:openfda.package_ndc
spl id		43f8fa10-9266-a4f3-e063-6394a90a9e93	id
spl set id		2bebe082-59b6-17c1-e063-6294a90a9a52	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 if allergic to iodine in the eyes Ask a doctor before use if injuries are deep or puncture wounds serious burn Stop use and ask doctor infection occurs redness, irritation or swelling develops Keep out of reach of children If swallowed, get medical help or contact Poison Control Center right away

Reported adverse events (FAERS/openFDA)#

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