warnings
Warnings For External Use Only
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 10%
- Manufacturer
- Humco Holding Group, Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 6064c23b-7c15-208d-e053-2991aa0a00f6
- SPL ID
- 0c936cb3-8393-0603-e063-6394a90a0640
- Version
- 7
- Effective date
- 2023-12-15
- Source export date
- 2026-10-12
- 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/2026-10-12/7928c8e8c6256620071a8b7e5b93eb8dfa543649c08d17a01ea02251012ba58c/drug-label-0001-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:27:12
| 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 10% | openfda.generic_name | |
| manufacturer name | Humco Holding Group, Inc. | openfda.manufacturer_name | |
| ndc | package | 0395-9123-16 | openfda.package_ndc |
| ndc | package | 0395-9123-98 | openfda.package_ndc |
| ndc | product | 0395-9123 | openfda.product_ndc |
| ndc11 | package | 00395912398 | derived:openfda.package_ndc |
| ndc11 | package | 00395912316 | derived:openfda.package_ndc |
| rxcui | 312564 | openfda.rxcui | |
| spl id | 0c936cb3-8393-0603-e063-6394a90a0640 | id | |
| spl set id | 6064c23b-7c15-208d-e053-2991aa0a00f6 | 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.