warnings
For external 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
- 3162c96a-061d-2971-e063-6394a90a9b74
- SPL ID
- 33f687f2-0c40-a498-e063-6294a90a58de
- Version
- 4
- Effective date
- 2025-04-29
- Source export date
- 2026-09-28
- Source partition
- 3
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:18:25
| 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 | 84165-002-25 | openfda.package_ndc |
| ndc | package | 84165-002-39 | openfda.package_ndc |
| ndc | package | 84165-002-35 | openfda.package_ndc |
| ndc | package | 84165-002-33 | openfda.package_ndc |
| ndc | package | 84165-002-30 | openfda.package_ndc |
| ndc | package | 84165-002-29 | openfda.package_ndc |
| ndc | package | 84165-002-52 | openfda.package_ndc |
| ndc | package | 84165-002-15 | openfda.package_ndc |
| ndc | package | 84165-002-49 | openfda.package_ndc |
| ndc | package | 84165-002-20 | openfda.package_ndc |
| ndc | package | 84165-002-01 | openfda.package_ndc |
| ndc | package | 84165-002-04 | openfda.package_ndc |
| ndc | package | 84165-002-28 | openfda.package_ndc |
| ndc | package | 84165-002-09 | openfda.package_ndc |
| ndc | package | 84165-002-21 | openfda.package_ndc |
| ndc | package | 84165-002-24 | openfda.package_ndc |
| ndc | package | 84165-002-37 | openfda.package_ndc |
| ndc | package | 84165-002-05 | openfda.package_ndc |
| ndc | package | 84165-002-17 | openfda.package_ndc |
| ndc | package | 84165-002-19 | openfda.package_ndc |
| ndc | package | 84165-002-07 | openfda.package_ndc |
| ndc | package | 84165-002-06 | openfda.package_ndc |
| ndc | package | 84165-002-41 | openfda.package_ndc |
| ndc | package | 84165-002-47 | openfda.package_ndc |
| ndc | package | 84165-002-27 | openfda.package_ndc |
| ndc | package | 84165-002-16 | openfda.package_ndc |
| ndc | package | 84165-002-18 | openfda.package_ndc |
| ndc | package | 84165-002-03 | openfda.package_ndc |
| ndc | package | 84165-002-40 | openfda.package_ndc |
| ndc | package | 84165-002-45 | openfda.package_ndc |
| ndc | package | 84165-002-38 | openfda.package_ndc |
| ndc | package | 84165-002-08 | openfda.package_ndc |
| ndc | package | 84165-002-31 | openfda.package_ndc |
| ndc | package | 84165-002-42 | openfda.package_ndc |
| ndc | package | 84165-002-53 | openfda.package_ndc |
| ndc | package | 84165-002-22 | 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.