Povidone Iodine Swabsticks 4 Triple

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 Swabsticks 4 Triple
Generic name
POVIDONE-IODINE
Manufacturer
Amsino healthcare (USA) inc.
Product type
HUMAN OTC DRUG
SPL set ID
45fdd9e3-031f-4741-868d-da606f60bb5a
SPL ID
09c727e0-0190-4b43-e063-6394a90abe69
Version
2
Effective date
2023-11-10
Source export date
2026-09-28
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/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:44:04
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 · 1 matching rows.

warnings

Warnings do not use if allergic to iodine do not use in the eyes Stop use and ask a doctor if redness,irritation,swelling or pain persists or increases infection occurs Keep out of reach of children. In case of accidental ingestion,seek professional assistance or consult a poison control center immediately. Avoid pooling beneath patient. Ask a doctor before use if injuries are For external use only. deep or puncture wounds serious burns

Reported adverse events (FAERS/openFDA)#

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