warnings
WARNINGS For external use only. Avoid contact with eyes. If irritation, sensitivity, or infection occurs, discontinue use. Keep out of reach of children.
LidoSpra
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
- LidoSpra
- Generic name
- LIDOSPRA
- Manufacturer
- Oncora Pharma, LLC
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 0f1a2c0d-d5d3-4b8f-94f6-0a01b4626959
- SPL ID
- 3b70d486-5f9e-4155-a206-a4de77c93b33
- Version
- 2
- Effective date
- 2026-08-25
- Source export date
- 2026-10-12
- Source partition
- 3
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/f40eac55ff4c5d55c3d8bbc5766ea7e21e4196960cfb4703b96a406b491c0cd5/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:32:43
| 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 |
|---|---|---|---|
| brand name | LidoSpra | openfda.brand_name | |
| generic name | LIDOSPRA | openfda.generic_name | |
| manufacturer name | Oncora Pharma, LLC | openfda.manufacturer_name | |
| ndc | package | 85477-325-29 | openfda.package_ndc |
| ndc | product | 85477-325 | openfda.product_ndc |
| ndc11 | package | 85477032529 | derived:openfda.package_ndc |
| rxcui | 2749997 | openfda.rxcui | |
| spl id | 3b70d486-5f9e-4155-a206-a4de77c93b33 | id | |
| spl set id | 0f1a2c0d-d5d3-4b8f-94f6-0a01b4626959 | set_id | |
| unii | 98PI200987 | 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.