warnings
Warnings For external use only
Plantar Pain Relief Patch
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
- Plantar Pain Relief Patch
- Generic name
- LIDOCAINE AND MENTHOL
- Manufacturer
- Guangzhou Sumi Technology Innovation Co., Ltd
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 4e8734db-e474-e1fa-e063-6394a90a3029
- SPL ID
- 51c4e080-64f2-dc0c-e063-6394a90a225d
- Version
- 2
- Effective date
- 2026-05-14
- Source export date
- 2026-09-28
- Source partition
- 10
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:07:24
| 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 | Plantar Pain Relief Patch | openfda.brand_name | |
| generic name | LIDOCAINE AND MENTHOL | openfda.generic_name | |
| manufacturer name | Guangzhou Sumi Technology Innovation Co., Ltd | openfda.manufacturer_name | |
| ndc | package | 87518-174-45 | openfda.package_ndc |
| ndc | package | 87518-174-15 | openfda.package_ndc |
| ndc | package | 87518-174-30 | openfda.package_ndc |
| ndc | package | 87518-174-01 | openfda.package_ndc |
| ndc | product | 87518-174 | openfda.product_ndc |
| ndc11 | package | 87518017401 | derived:openfda.package_ndc |
| ndc11 | package | 87518017445 | derived:openfda.package_ndc |
| ndc11 | package | 87518017415 | derived:openfda.package_ndc |
| ndc11 | package | 87518017430 | derived:openfda.package_ndc |
| rxcui | 1249758 | openfda.rxcui | |
| spl id | 51c4e080-64f2-dc0c-e063-6394a90a225d | id | |
| spl set id | 4e8734db-e474-e1fa-e063-6394a90a3029 | set_id | |
| unii | 98PI200987 | openfda.unii | |
| unii | L7T10EIP3A | 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.