warnings
For external use only
FOOT PAIN RELIEF ROLL-ON
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
- FOOT PAIN RELIEF ROLL-ON
- Generic name
- LIDOCAINE, MENTHOL
- Manufacturer
- Guangzhou Zhupuyou E-commerce Co., Ltd
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 43edcea0-ab04-f368-e063-6294a90a817a
- SPL ID
- 43edcea0-ab05-f368-e063-6294a90a817a
- Version
- 1
- Effective date
- 2025-11-19
- Source export date
- 2026-10-12
- Source partition
- 6
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/b25dad4aaef9c88f0e827394a34fbbd1ce7d71422fa46b5d1e123befad498c1d/drug-label-0006-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:45:08
| 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 | FOOT PAIN RELIEF ROLL-ON | openfda.brand_name | |
| generic name | LIDOCAINE, MENTHOL | openfda.generic_name | |
| manufacturer name | Guangzhou Zhupuyou E-commerce Co., Ltd | openfda.manufacturer_name | |
| ndc | package | 84165-017-08 | openfda.package_ndc |
| ndc | package | 84165-017-02 | openfda.package_ndc |
| ndc | package | 84165-017-01 | openfda.package_ndc |
| ndc | package | 84165-017-03 | openfda.package_ndc |
| ndc | package | 84165-017-05 | openfda.package_ndc |
| ndc | package | 84165-017-06 | openfda.package_ndc |
| ndc | package | 84165-017-07 | openfda.package_ndc |
| ndc | package | 84165-017-09 | openfda.package_ndc |
| ndc | package | 84165-017-10 | openfda.package_ndc |
| ndc | package | 84165-017-04 | openfda.package_ndc |
| ndc | product | 84165-017 | openfda.product_ndc |
| ndc11 | package | 84165001703 | derived:openfda.package_ndc |
| ndc11 | package | 84165001702 | derived:openfda.package_ndc |
| ndc11 | package | 84165001707 | derived:openfda.package_ndc |
| ndc11 | package | 84165001704 | derived:openfda.package_ndc |
| ndc11 | package | 84165001710 | derived:openfda.package_ndc |
| ndc11 | package | 84165001708 | derived:openfda.package_ndc |
| ndc11 | package | 84165001706 | derived:openfda.package_ndc |
| ndc11 | package | 84165001705 | derived:openfda.package_ndc |
| ndc11 | package | 84165001701 | derived:openfda.package_ndc |
| ndc11 | package | 84165001709 | derived:openfda.package_ndc |
| rxcui | 252967 | openfda.rxcui | |
| spl id | 43edcea0-ab05-f368-e063-6294a90a817a | id | |
| spl set id | 43edcea0-ab04-f368-e063-6294a90a817a | 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.