warnings
For external use only
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
- PAIN RELIEF Gel-Patch
- Generic name
- LIDOCAINE, MENTHOL
- Manufacturer
- Guangzhou Zhupuyou E-commerce Co., Ltd
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 22d9ce20-1cb6-c5bd-e063-6394a90a9eca
- SPL ID
- 47db7f81-d850-5672-e063-6294a90aae8a
- Version
- 2
- Effective date
- 2026-01-08
- Source export date
- 2026-09-28
- Source partition
- 2
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:15:20
| 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 | 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 | 84165-104-45 | openfda.package_ndc |
| ndc | package | 84165-104-31 | openfda.package_ndc |
| ndc | package | 84165-104-38 | openfda.package_ndc |
| ndc | package | 84165-104-01 | openfda.package_ndc |
| ndc | package | 84165-104-37 | openfda.package_ndc |
| ndc | package | 84165-104-13 | openfda.package_ndc |
| ndc | package | 84165-104-53 | openfda.package_ndc |
| ndc | package | 84165-104-39 | openfda.package_ndc |
| ndc | package | 84165-104-23 | openfda.package_ndc |
| ndc | package | 84165-104-41 | openfda.package_ndc |
| ndc | package | 84165-104-32 | openfda.package_ndc |
| ndc | package | 84165-104-08 | openfda.package_ndc |
| ndc | package | 84165-104-51 | openfda.package_ndc |
| ndc | package | 84165-104-21 | openfda.package_ndc |
| ndc | package | 84165-104-35 | openfda.package_ndc |
| ndc | package | 84165-104-44 | openfda.package_ndc |
| ndc | package | 84165-104-47 | openfda.package_ndc |
| ndc | package | 84165-104-48 | openfda.package_ndc |
| ndc | package | 84165-104-49 | openfda.package_ndc |
| ndc | package | 84165-104-18 | openfda.package_ndc |
| ndc | package | 84165-104-54 | openfda.package_ndc |
| ndc | package | 84165-104-40 | openfda.package_ndc |
| ndc | package | 84165-104-09 | openfda.package_ndc |
| ndc | package | 84165-104-24 | openfda.package_ndc |
| ndc | package | 84165-104-17 | openfda.package_ndc |
| ndc | package | 84165-104-29 | openfda.package_ndc |
| ndc | package | 84165-104-22 | openfda.package_ndc |
| ndc | package | 84165-104-30 | openfda.package_ndc |
| ndc | package | 84165-104-15 | openfda.package_ndc |
| ndc | package | 84165-104-14 | openfda.package_ndc |
| ndc | package | 84165-104-46 | openfda.package_ndc |
| ndc | package | 84165-104-07 | openfda.package_ndc |
| ndc | package | 84165-104-43 | openfda.package_ndc |
| ndc | package | 84165-104-05 | openfda.package_ndc |
| ndc | package | 84165-104-11 | openfda.package_ndc |
| ndc | package | 84165-104-28 | 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.