warnings
For external use only
Lidocaine Knee 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
- Lidocaine Knee Pain Relief Gel-Patch
- Generic name
- LIDOCAINE
- Manufacturer
- Guangzhou Zhupuyou E-commerce Co., Ltd
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 384c1ff8-80bd-86cb-e063-6394a90a2d65
- SPL ID
- 384c1ff8-80be-86cb-e063-6394a90a2d65
- Version
- 1
- Effective date
- 2025-06-24
- Source export date
- 2026-09-28
- Source partition
- 8
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:54:11
| 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 | Lidocaine Knee Pain Relief Gel-Patch | openfda.brand_name | |
| generic name | LIDOCAINE | openfda.generic_name | |
| manufacturer name | Guangzhou Zhupuyou E-commerce Co., Ltd | openfda.manufacturer_name | |
| ndc | package | 84165-014-28 | openfda.package_ndc |
| ndc | package | 84165-014-16 | openfda.package_ndc |
| ndc | package | 84165-014-12 | openfda.package_ndc |
| ndc | package | 84165-014-50 | openfda.package_ndc |
| ndc | package | 84165-014-27 | openfda.package_ndc |
| ndc | package | 84165-014-25 | openfda.package_ndc |
| ndc | package | 84165-014-01 | openfda.package_ndc |
| ndc | package | 84165-014-07 | openfda.package_ndc |
| ndc | package | 84165-014-35 | openfda.package_ndc |
| ndc | package | 84165-014-22 | openfda.package_ndc |
| ndc | package | 84165-014-48 | openfda.package_ndc |
| ndc | package | 84165-014-24 | openfda.package_ndc |
| ndc | package | 84165-014-21 | openfda.package_ndc |
| ndc | package | 84165-014-18 | openfda.package_ndc |
| ndc | package | 84165-014-46 | openfda.package_ndc |
| ndc | package | 84165-014-23 | openfda.package_ndc |
| ndc | package | 84165-014-54 | openfda.package_ndc |
| ndc | package | 84165-014-55 | openfda.package_ndc |
| ndc | package | 84165-014-29 | openfda.package_ndc |
| ndc | package | 84165-014-05 | openfda.package_ndc |
| ndc | package | 84165-014-32 | openfda.package_ndc |
| ndc | package | 84165-014-10 | openfda.package_ndc |
| ndc | package | 84165-014-08 | openfda.package_ndc |
| ndc | package | 84165-014-20 | openfda.package_ndc |
| ndc | package | 84165-014-56 | openfda.package_ndc |
| ndc | package | 84165-014-37 | openfda.package_ndc |
| ndc | package | 84165-014-45 | openfda.package_ndc |
| ndc | package | 84165-014-11 | openfda.package_ndc |
| ndc | package | 84165-014-51 | openfda.package_ndc |
| ndc | package | 84165-014-43 | openfda.package_ndc |
| ndc | package | 84165-014-06 | openfda.package_ndc |
| ndc | package | 84165-014-14 | openfda.package_ndc |
| ndc | package | 84165-014-26 | openfda.package_ndc |
| ndc | package | 84165-014-33 | openfda.package_ndc |
| ndc | package | 84165-014-47 | openfda.package_ndc |
| ndc | package | 84165-014-40 | 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.