Aplicare 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: Aplicare Povidone-Iodine
Generic name: POVIDONE-IODINE
Manufacturer: Aplicare Products, LLC
Product type: HUMAN OTC DRUG
SPL set ID: 7302a2f8-a600-4200-bc4e-309e4c190fe5
SPL ID: 5a86eb3c-9bed-842f-e063-6294a90adff3
Version: 20
Effective date: 2026-09-02
Source export date: 2026-10-27
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/977776a6cc37ec1c77259da8a93ae161850a3aa120341096e5a03428b84d016b/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 21:00:27

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 · 26 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		Aplicare Povidone-Iodine	openfda.brand_name
generic name		POVIDONE-IODINE	openfda.generic_name
manufacturer name		Aplicare Products, LLC	openfda.manufacturer_name
ndc	package	52380-1905-7	openfda.package_ndc
ndc	package	52380-1905-9	openfda.package_ndc
ndc	package	52380-1905-0	openfda.package_ndc
ndc	package	52380-1905-3	openfda.package_ndc
ndc	package	52380-1905-8	openfda.package_ndc
ndc	package	52380-1905-4	openfda.package_ndc
ndc	package	52380-1905-6	openfda.package_ndc
ndc	package	52380-1905-2	openfda.package_ndc
ndc	product	52380-1905	openfda.product_ndc
ndc11	package	52380190502	derived:openfda.package_ndc
ndc11	package	52380190509	derived:openfda.package_ndc
ndc11	package	52380190504	derived:openfda.package_ndc
ndc11	package	52380190508	derived:openfda.package_ndc
ndc11	package	52380190507	derived:openfda.package_ndc
ndc11	package	52380190500	derived:openfda.package_ndc
ndc11	package	52380190506	derived:openfda.package_ndc
ndc11	package	52380190503	derived:openfda.package_ndc
rxcui		617973	openfda.rxcui
rxcui		312564	openfda.rxcui
spl id		5a86eb3c-9bed-842f-e063-6294a90adff3	id
spl set id		7302a2f8-a600-4200-bc4e-309e4c190fe5	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 Avoid "pooling" beneath patient. Prolonged exposure to wet solution may cause skin irritation. Do not use in the eyes on individuals allergic or sensitive to iodine Ask a doctor before use if injuries are deep or puncture wounds serious burns Stop use and ask a doctor if infection occurs redness, irritation, swelling or pain persists or increases Keep out of reach of children. In case of accidental ingestion, seek professional assistance or consult a poison control center immediately.

Reported adverse events (FAERS/openFDA)#

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