FDA.reportPublic FDA data

Aplicare

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
Generic name
POVIDONE-IODINE
Manufacturer
Aplicare Products LLC
Product type
HUMAN OTC DRUG
SPL set ID
0a48b8ef-f2d6-ed50-e063-6394a90a8ebe
SPL ID
4640ae81-0ef8-0677-e063-6394a90a5a89
Version
3
Effective date
2025-12-18
Source export date
2026-09-28
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/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:26:38
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 2 matching rows.

warnings

Warnings For external use only Do not use if allergic to iodine in the eyes Stop use and ask a doctor if redness, irritation, swelling or pain develops or persists for more than 72 hours infection occurs Keep out of reach of children. In case of accidental ingestion, seek professional assistance or consult a poison control center immediately.

warnings

Stop use and ask a doctor if redness, irritation, swelling or pain develops or persists for more than 72 hours infection occurs

Reported adverse events (FAERS/openFDA)#

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