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
- 32b96689-8e9b-4c2e-e063-6294a90a7d1c
- SPL ID
- 33f5f00c-263f-883a-e063-6394a90acdf7
- Version
- 2
- Effective date
- 2025-04-29
- Source export date
- 2026-09-28
- Source partition
- 9
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/6784607726c827491ceaeab30d843632e0660ee8008c535197be5ed9e1e52201/drug-label-0009-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:04:45
| 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 | 84165-006-06 | openfda.package_ndc |
| ndc | package | 84165-006-31 | openfda.package_ndc |
| ndc | package | 84165-006-45 | openfda.package_ndc |
| ndc | package | 84165-006-17 | openfda.package_ndc |
| ndc | package | 84165-006-11 | openfda.package_ndc |
| ndc | package | 84165-006-58 | openfda.package_ndc |
| ndc | package | 84165-006-47 | openfda.package_ndc |
| ndc | package | 84165-006-28 | openfda.package_ndc |
| ndc | package | 84165-006-37 | openfda.package_ndc |
| ndc | package | 84165-006-29 | openfda.package_ndc |
| ndc | package | 84165-006-23 | openfda.package_ndc |
| ndc | package | 84165-002-01 | openfda.package_ndc |
| ndc | package | 84165-107-01 | openfda.package_ndc |
| ndc | package | 84165-006-41 | openfda.package_ndc |
| ndc | package | 84165-006-54 | openfda.package_ndc |
| ndc | package | 84165-006-57 | openfda.package_ndc |
| ndc | package | 84165-006-38 | openfda.package_ndc |
| ndc | package | 84165-006-27 | openfda.package_ndc |
| ndc | package | 84165-006-35 | openfda.package_ndc |
| ndc | package | 84165-006-25 | openfda.package_ndc |
| ndc | package | 84165-006-30 | openfda.package_ndc |
| ndc | package | 84165-006-59 | openfda.package_ndc |
| ndc | package | 84165-006-09 | openfda.package_ndc |
| ndc | package | 84165-006-44 | openfda.package_ndc |
| ndc | package | 84165-006-60 | openfda.package_ndc |
| ndc | package | 84165-006-20 | openfda.package_ndc |
| ndc | package | 84165-006-49 | openfda.package_ndc |
| ndc | package | 84165-006-34 | openfda.package_ndc |
| ndc | package | 84165-006-46 | openfda.package_ndc |
| ndc | package | 84165-006-56 | openfda.package_ndc |
| ndc | package | 84165-006-50 | openfda.package_ndc |
| ndc | package | 84165-006-15 | openfda.package_ndc |
| ndc | package | 84165-006-43 | openfda.package_ndc |
| ndc | package | 84165-005-01 | openfda.package_ndc |
| ndc | package | 84165-006-26 | openfda.package_ndc |
| ndc | package | 84165-006-36 | 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.