warnings
Warnings For external use only
Lidocaine Pain Relieve 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 Relieve Gel-Patch
- Generic name
- PAIN RELIEVE GEL-PATCH
- Manufacturer
- Henan Kangdi Medical Devices Co., Ltd
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 1e31b950-e990-e255-e063-6394a90a7d23
- SPL ID
- 4a37ed9c-5f8b-ad8b-e063-6394a90ac527
- Version
- 3
- Effective date
- 2026-02-07
- 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 05:14:58
| 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 Relieve Gel-Patch | openfda.brand_name | |
| generic name | PAIN RELIEVE GEL-PATCH | openfda.generic_name | |
| manufacturer name | Henan Kangdi Medical Devices Co., Ltd | openfda.manufacturer_name | |
| ndc | package | 69561-005-01 | openfda.package_ndc |
| ndc | package | 69561-005-03 | openfda.package_ndc |
| ndc | package | 69561-005-02 | openfda.package_ndc |
| ndc | product | 69561-005 | openfda.product_ndc |
| ndc11 | package | 69561000501 | derived:openfda.package_ndc |
| ndc11 | package | 69561000502 | derived:openfda.package_ndc |
| ndc11 | package | 69561000503 | derived:openfda.package_ndc |
| rxcui | 1737778 | openfda.rxcui | |
| spl id | 4a37ed9c-5f8b-ad8b-e063-6394a90ac527 | id | |
| spl set id | 1e31b950-e990-e255-e063-6394a90a7d23 | set_id | |
| unii | 98PI200987 | openfda.unii |
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.