warnings
For external use only
Plantar Fasciitis Pain Relief Gel-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 Fasciitis Pain Relief Gel-Patch
- Generic name
- LIDOCAINE, MENTHOL
- Manufacturer
- Guangzhou Zhupuyou E-commerce Co., Ltd
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 34838622-b092-afeb-e063-6294a90ae7db
- SPL ID
- 34838622-b093-afeb-e063-6294a90ae7db
- Version
- 1
- Effective date
- 2025-05-06
- Source export date
- 2026-09-28
- 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/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:37:10
| 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 | Plantar Fasciitis Pain Relief Gel-Patch | openfda.brand_name | |
| generic name | LIDOCAINE, MENTHOL | openfda.generic_name | |
| manufacturer name | Guangzhou Zhupuyou E-commerce Co., Ltd | openfda.manufacturer_name | |
| ndc | package | 84165-007-27 | openfda.package_ndc |
| ndc | package | 84165-007-15 | openfda.package_ndc |
| ndc | package | 84165-007-23 | openfda.package_ndc |
| ndc | package | 84165-007-52 | openfda.package_ndc |
| ndc | package | 84165-007-31 | openfda.package_ndc |
| ndc | package | 84165-007-42 | openfda.package_ndc |
| ndc | package | 84165-007-44 | openfda.package_ndc |
| ndc | package | 84165-007-25 | openfda.package_ndc |
| ndc | package | 84165-007-51 | openfda.package_ndc |
| ndc | package | 84165-007-16 | openfda.package_ndc |
| ndc | package | 84165-007-46 | openfda.package_ndc |
| ndc | package | 84165-007-13 | openfda.package_ndc |
| ndc | package | 84165-007-41 | openfda.package_ndc |
| ndc | package | 84165-007-49 | openfda.package_ndc |
| ndc | package | 84165-007-21 | openfda.package_ndc |
| ndc | package | 84165-007-28 | openfda.package_ndc |
| ndc | package | 84165-007-53 | openfda.package_ndc |
| ndc | package | 84165-007-45 | openfda.package_ndc |
| ndc | package | 84165-007-24 | openfda.package_ndc |
| ndc | package | 84165-007-19 | openfda.package_ndc |
| ndc | package | 84165-007-05 | openfda.package_ndc |
| ndc | package | 84165-007-55 | openfda.package_ndc |
| ndc | package | 84165-007-37 | openfda.package_ndc |
| ndc | package | 84165-007-14 | openfda.package_ndc |
| ndc | package | 84165-007-18 | openfda.package_ndc |
| ndc | package | 84165-007-29 | openfda.package_ndc |
| ndc | package | 84165-007-32 | openfda.package_ndc |
| ndc | package | 84165-007-43 | openfda.package_ndc |
| ndc | package | 84165-007-06 | openfda.package_ndc |
| ndc | package | 84165-007-08 | openfda.package_ndc |
| ndc | package | 84165-007-20 | openfda.package_ndc |
| ndc | package | 84165-007-17 | openfda.package_ndc |
| ndc | package | 84165-007-09 | openfda.package_ndc |
| ndc | package | 84165-007-07 | openfda.package_ndc |
| ndc | package | 84165-007-50 | openfda.package_ndc |
| ndc | package | 84165-007-39 | openfda.package_ndc |
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.