Povidone-Iodine Prep Pad

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 Prep Pad
Generic name: POVIDONE-IODINE
Manufacturer: Cardinal Health 200, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 06c8a6f6-2fc8-4292-a3b5-6311a918a521
SPL ID: 085ebaa7-2663-90e3-e063-6294a90a8a56
Version: 5
Effective date: 2023-10-23
Source export date: 2026-10-27
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/d7629e6f844435cfe6cb0cf8c5341c46775ea16c5af42c77a22a2ffe820a2cd2/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 19:48:54

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 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M003	openfda.application_number
brand name		Povidone-Iodine Prep Pad	openfda.brand_name
generic name		POVIDONE-IODINE	openfda.generic_name
manufacturer name		Cardinal Health 200, Inc.	openfda.manufacturer_name
ndc	package	63517-400-83	openfda.package_ndc
ndc	product	63517-400	openfda.product_ndc
ndc11	package	63517040083	derived:openfda.package_ndc
rxcui		797730	openfda.rxcui
spl id		085ebaa7-2663-90e3-e063-6294a90a8a56	id
spl set id		06c8a6f6-2fc8-4292-a3b5-6311a918a521	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 apply to persons allergic to Iodine Allergy Alert: Do not use • in the eyes or apply over large areas of the body • longer than one week unless directed by a doctor Ask a doctor before use if you have • deep or puncture wounds • animal bites • serious burns Stop use and consult a doctor if the condition persists or gets worse Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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