warnings
Warnings For external use only. Ask a doctor before use if you have • deep or puncture wounds • serious burns Stop use and ask a doctor if • redness, irritation, swelling or pain persists or increases • infection occurs.
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
- Brand name
- POVIDONE-IODINE
- Generic name
- POVIDONE-IODINE
- Manufacturer
- James Alexander Corporation
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 181a6363-2249-45f0-a28b-79f2c5ffad59
- SPL ID
- a0c3cfbd-f346-4c1b-be91-c04b077c4bd3
- Version
- 9
- Effective date
- 2025-10-23
- Source export date
- 2026-11-06
- Source partition
- 8
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-11-06/db89d5ebfc3e02f44e8769334d799cd3436b05f779823ab00297f1f800c89ddf/drug-label-0008-of-0014.json.zip
- Source manifest SHA-256
- 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
- Import run
- 20261108T063105Z
- Imported at
- 2026-11-08 07:35:42
| 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.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| application number | M003 | openfda.application_number | |
| brand name | POVIDONE-IODINE | openfda.brand_name | |
| generic name | POVIDONE-IODINE | openfda.generic_name | |
| manufacturer name | James Alexander Corporation | openfda.manufacturer_name | |
| ndc | package | 46414-7777-3 | openfda.package_ndc |
| ndc | package | 46414-7777-2 | openfda.package_ndc |
| ndc | product | 46414-7777 | openfda.product_ndc |
| ndc11 | package | 46414777703 | derived:openfda.package_ndc |
| ndc11 | package | 46414777702 | derived:openfda.package_ndc |
| rxcui | 312564 | openfda.rxcui | |
| spl id | a0c3cfbd-f346-4c1b-be91-c04b077c4bd3 | id | |
| spl set id | 181a6363-2249-45f0-a28b-79f2c5ffad59 | set_id | |
| unii | 85H0HZU99M | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.