warnings
Warnings For external use only If swallowed, get medical help or contact a Poison Control Center. Discontinue use if irritation and redness develop. If condition persist for more than 72 hours or gets worse, consult a healthcare provider
PVP Iodine Prep Pad Medium and Large
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
- PVP Iodine Prep Pad Medium and Large
- Generic name
- PROVIDONE IODINE
- Manufacturer
- Professional Disposables International, Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 50c524ab-7029-494a-8bb4-d90a4d184fb2
- SPL ID
- 57eef33c-3427-2811-e063-6394a90adfff
- Version
- 13
- Effective date
- 2026-07-31
- Source export date
- 2026-09-28
- Source partition
- 2
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:15:27
| 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 | 505G(a)(3) | openfda.application_number | |
| brand name | PVP Iodine Prep Pad Medium and Large | openfda.brand_name | |
| brand name | PVP Iodine Prep Swabstick Ones and Threes | openfda.brand_name | |
| generic name | PROVIDONE IODINE | openfda.generic_name | |
| manufacturer name | Professional Disposables International, Inc. | openfda.manufacturer_name | |
| ndc | package | 10819-3883-1 | openfda.package_ndc |
| ndc | package | 10819-3885-2 | openfda.package_ndc |
| ndc | package | 10819-3883-3 | openfda.package_ndc |
| ndc | package | 10819-3885-1 | openfda.package_ndc |
| ndc | product | 10819-3885 | openfda.product_ndc |
| ndc | product | 10819-3883 | openfda.product_ndc |
| ndc11 | package | 10819388303 | derived:openfda.package_ndc |
| ndc11 | package | 10819388301 | derived:openfda.package_ndc |
| ndc11 | package | 10819388501 | derived:openfda.package_ndc |
| ndc11 | package | 10819388502 | derived:openfda.package_ndc |
| rxcui | 797730 | openfda.rxcui | |
| spl id | 57eef33c-3427-2811-e063-6394a90adfff | id | |
| spl set id | 50c524ab-7029-494a-8bb4-d90a4d184fb2 | 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.