warnings
Warnings For external use only
Betadine Solution
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
- Betadine Solution
- Generic name
- POVIDONE-IODINE
- Manufacturer
- Atlantis Consumer Healthcare, Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 41891599-420e-48d2-8e31-d28a2209e383
- SPL ID
- 81830efd-5944-490f-86cf-90add1fdd2e3
- Version
- 11
- Effective date
- 2025-01-06
- Source export date
- 2026-09-28
- Source partition
- 11
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:19:16
| 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 | Betadine Solution | openfda.brand_name | |
| generic name | POVIDONE-IODINE | openfda.generic_name | |
| manufacturer name | Atlantis Consumer Healthcare, Inc. | openfda.manufacturer_name | |
| ndc | package | 67618-150-32 | openfda.package_ndc |
| ndc | package | 67618-150-01 | openfda.package_ndc |
| ndc | package | 67618-150-05 | openfda.package_ndc |
| ndc | package | 67618-150-09 | openfda.package_ndc |
| ndc | package | 67618-150-17 | openfda.package_ndc |
| ndc | package | 67618-150-04 | openfda.package_ndc |
| ndc | product | 67618-150 | openfda.product_ndc |
| ndc11 | package | 67618015004 | derived:openfda.package_ndc |
| ndc11 | package | 67618015005 | derived:openfda.package_ndc |
| ndc11 | package | 67618015017 | derived:openfda.package_ndc |
| ndc11 | package | 67618015009 | derived:openfda.package_ndc |
| ndc11 | package | 67618015032 | derived:openfda.package_ndc |
| ndc11 | package | 67618015001 | derived:openfda.package_ndc |
| rxcui | 211108 | openfda.rxcui | |
| rxcui | 312564 | openfda.rxcui | |
| spl id | 81830efd-5944-490f-86cf-90add1fdd2e3 | id | |
| spl set id | 41891599-420e-48d2-8e31-d28a2209e383 | 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.