Aplicare Povidone-iodine Scrub

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 Scrub
Generic name
POVIDONE-IODINE
Manufacturer
Aplicare Products, LLC
Product type
HUMAN OTC DRUG
SPL set ID
ff19ea2f-d6a0-442f-8f23-d559fc13c549
SPL ID
5693416a-3567-5978-e063-6294a90a5ea7
Version
12
Effective date
2026-07-14
Source export date
2026-10-12
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/2026-10-12/edd23646015c9adc800cdbe2b778398a2d2b70e90dce5721ef2b191499a0397f/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:56:29
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

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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, or 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.