warnings
LidoSync Warnings Do Not Use Do not use on large areas of the body or on cut, irritated or swollen skin on puncture wounds for more than one week without consulting a doctor
LidoSync
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
- LidoSync
- Generic name
- LIDOCAINE, MENTHOL
- Manufacturer
- iON Pharma, LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 200f883c-439a-3b99-e063-6394a90aed10
- SPL ID
- 200f883c-439b-3b99-e063-6394a90aed10
- Version
- 1
- Effective date
- 2024-08-19
- Source export date
- 2026-09-28
- 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/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:47:58
| 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 | M017 | openfda.application_number | |
| brand name | LidoSync | openfda.brand_name | |
| generic name | LIDOCAINE, MENTHOL | openfda.generic_name | |
| manufacturer name | iON Pharma, LLC | openfda.manufacturer_name | |
| ndc | package | 82944-200-01 | openfda.package_ndc |
| ndc | product | 82944-200 | openfda.product_ndc |
| ndc11 | package | 82944020001 | derived:openfda.package_ndc |
| spl id | 200f883c-439b-3b99-e063-6394a90aed10 | id | |
| spl set id | 200f883c-439a-3b99-e063-6394a90aed10 | set_id | |
| unii | BZ1R15MTK7 | openfda.unii | |
| unii | EC2CNF7XFP | 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.