warnings
For extemal use only
Lidocaine 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 Pain Relief Gel-Patch
- Generic name
- LIDOCAINE
- Manufacturer
- Guangzhou Zhupuyou E-commerce Co., Ltd
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 296fcc36-563f-19ca-e063-6394a90ab3ae
- SPL ID
- 2bb9b5c9-997b-fd18-e063-6394a90ad80b
- Version
- 3
- Effective date
- 2025-01-15
- Source export date
- 2026-09-28
- Source partition
- 5
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:27:48
| 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 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 | 84165-106-20 | openfda.package_ndc |
| ndc | package | 84165-106-15 | openfda.package_ndc |
| ndc | package | 84165-106-53 | openfda.package_ndc |
| ndc | package | 84165-106-33 | openfda.package_ndc |
| ndc | package | 84165-106-49 | openfda.package_ndc |
| ndc | package | 84165-106-06 | openfda.package_ndc |
| ndc | package | 84165-106-55 | openfda.package_ndc |
| ndc | package | 84165-106-46 | openfda.package_ndc |
| ndc | package | 84165-106-01 | openfda.package_ndc |
| ndc | package | 84165-106-43 | openfda.package_ndc |
| ndc | package | 84165-106-23 | openfda.package_ndc |
| ndc | package | 84165-106-09 | openfda.package_ndc |
| ndc | package | 84165-106-40 | openfda.package_ndc |
| ndc | package | 84165-106-29 | openfda.package_ndc |
| ndc | package | 84165-106-38 | openfda.package_ndc |
| ndc | package | 84165-106-35 | openfda.package_ndc |
| ndc | package | 84165-106-22 | openfda.package_ndc |
| ndc | package | 84165-106-42 | openfda.package_ndc |
| ndc | package | 84165-106-47 | openfda.package_ndc |
| ndc | package | 84165-106-34 | openfda.package_ndc |
| ndc | package | 84165-106-26 | openfda.package_ndc |
| ndc | package | 84165-106-44 | openfda.package_ndc |
| ndc | package | 84165-106-18 | openfda.package_ndc |
| ndc | package | 84165-106-45 | openfda.package_ndc |
| ndc | package | 84165-106-19 | openfda.package_ndc |
| ndc | package | 84165-106-05 | openfda.package_ndc |
| ndc | package | 84165-106-30 | openfda.package_ndc |
| ndc | package | 84165-106-51 | openfda.package_ndc |
| ndc | package | 84165-106-27 | openfda.package_ndc |
| ndc | package | 84165-106-28 | openfda.package_ndc |
| ndc | package | 84165-106-12 | openfda.package_ndc |
| ndc | package | 84165-106-17 | openfda.package_ndc |
| ndc | package | 84165-106-16 | openfda.package_ndc |
| ndc | package | 84165-106-41 | openfda.package_ndc |
| ndc | package | 84165-106-31 | openfda.package_ndc |
| ndc | package | 84165-106-25 | 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.