Freskaro Decolorized 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
Freskaro Decolorized Iodine
Generic name
ALCOHOL
Manufacturer
Pharma Nobis, LLC
Product type
HUMAN OTC DRUG
SPL set ID
fbd222a2-1151-99b9-e053-6394a90a8bb8
SPL ID
0d99d51f-ba65-9536-e063-6394a90aecd3
Version
2
Effective date
2023-12-28
Source export date
2026-09-28
Source partition
1
Source file
https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/9c7783846d422acb0c9e59457606951c785a7d28cc631c8cc4839d0dc7c55f39/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:14:05
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 When using the product Do not use in the eyes or apply over large areas of the bosy. In case of deep or puncture wounds, animal bites or serious burns, consult a doctor. Stop use and consult a doctor if the condition persists or gets worse. Do not use this product for longer than 1 week unless directed by a doctor. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately. Soap will deactivate the effects of this product.

warnings and cautions

When using the product Do not use in the eyes or apply over large areas of the bosy. In case of deep or puncture wounds, animal bites or serious burns, consult a doctor.

Reported adverse events (FAERS/openFDA)#

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