Povidone Iodine

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
Generic name: POVIDONE-IODINE
Manufacturer: Dr Radows
Product type: HUMAN OTC DRUG
SPL set ID: 58e1757c-45ce-455e-bd64-a9e99cd3680f
SPL ID: 7bad4367-4449-46e9-8e5a-61296bc466fd
Version: 2
Effective date: 2023-10-30
Source export date: 2026-10-12
Source partition: 7
Source file: https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/ff22b88bd32e56cbc369af80345075227138a42b1b3ba9a84f038fd5493a7a47/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:54:29

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		M005	openfda.application_number
brand name		Povidone Iodine	openfda.brand_name
generic name		POVIDONE-IODINE	openfda.generic_name
manufacturer name		Dr Radows	openfda.manufacturer_name
ndc	package	81584-1102-1	openfda.package_ndc
ndc	product	81584-1102	openfda.product_ndc
ndc11	package	81584110201	derived:openfda.package_ndc
rxcui		312563	openfda.rxcui
spl id		7bad4367-4449-46e9-8e5a-61296bc466fd	id
spl set id		58e1757c-45ce-455e-bd64-a9e99cd3680f	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 over large areas of the body if you are allergic to any of the ingredients longer than 1 week unless directed by a doctor When using this product Avoid contact with eyes. Ask a doctor before use if you have deep or puncture wounds animal bites serious burns Stop use and ask a doctor if redness, irritation or swelling occurs or pain persists Keep this and all drugs out of the reach of children. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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