warnings
Warnings: Do not use if allergic to iodine For external use only
Lights Povidone Iodine Scrub
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
- Lights Povidone Iodine Scrub
- Generic name
- POVIDONE-IODINE
- Manufacturer
- Lights Medical Manufacture Co., Ltd.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 5e1eef53-c2c7-477e-9ee4-19c01c1881e5
- SPL ID
- 359b63c4-7d46-5d16-e063-6294a90a99fa
- Version
- 1
- Effective date
- 2025-05-20
- Source export date
- 2026-10-27
- Source partition
- 7
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-27/be847f9aea8d80a2cb7e9771acd1143be084664192ecf8f5be8ac1024116f4f0/drug-label-0007-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 20:16:42
| 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 | M004 | openfda.application_number | |
| brand name | Lights Povidone Iodine Scrub | openfda.brand_name | |
| generic name | POVIDONE-IODINE | openfda.generic_name | |
| manufacturer name | Lights Medical Manufacture Co., Ltd. | openfda.manufacturer_name | |
| ndc | package | 61333-216-01 | openfda.package_ndc |
| ndc | product | 61333-216 | openfda.product_ndc |
| ndc11 | package | 61333021601 | derived:openfda.package_ndc |
| rxcui | 314188 | openfda.rxcui | |
| spl id | 359b63c4-7d46-5d16-e063-6294a90a99fa | id | |
| spl set id | 5e1eef53-c2c7-477e-9ee4-19c01c1881e5 | 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.