First Aid Only Povidone-Iodine Antiseptic

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: First Aid Only Povidone-Iodine Antiseptic
Generic name: POVIDONE-IODINE
Manufacturer: Acme United Corporation
Product type: HUMAN OTC DRUG
SPL set ID: e0052ac2-4f74-32a4-e053-2995a90a94c6
SPL ID: 1f93db77-6db7-9866-e063-6394a90aa068
Version: 2
Effective date: 2024-08-13
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 05:16:01

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 · 16 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M003	openfda.application_number
brand name		First Aid Only Povidone-Iodine Antiseptic	openfda.brand_name
generic name		POVIDONE-IODINE	openfda.generic_name
manufacturer name		Acme United Corporation	openfda.manufacturer_name
ndc	package	0924-8113-00	openfda.package_ndc
ndc	package	0924-8113-02	openfda.package_ndc
ndc	package	0924-8113-01	openfda.package_ndc
ndc	package	0924-8113-03	openfda.package_ndc
ndc	product	0924-8113	openfda.product_ndc
ndc11	package	00924811303	derived:openfda.package_ndc
ndc11	package	00924811300	derived:openfda.package_ndc
ndc11	package	00924811301	derived:openfda.package_ndc
ndc11	package	00924811302	derived:openfda.package_ndc
spl id		1f93db77-6db7-9866-e063-6394a90aa068	id
spl set id		e0052ac2-4f74-32a4-e053-2995a90a94c6	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 eyes ▪ over large areas of the body ▪ if allergic to any of the ingredients ▪ longer than 1 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 ask a doctor if ▪ conditions worsen or clear up and then recur ▪ the condition persists for more than 7 days 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.