warnings
Warnings For external use only
Knee 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
- Knee Pain Relief Gel-Patch
- Generic name
- LIDOCAINE AND MENTHOL
- Manufacturer
- Guangzhou Liuquanmiao Import & Export Trade Co., Ltd.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 54071b61-6e69-03e3-e063-6394a90a42f0
- SPL ID
- 54071db0-8180-ffe6-e063-6394a90a8625
- Version
- 1
- Effective date
- 2026-06-11
- Source export date
- 2026-09-28
- Source partition
- 12
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:27:44
| 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 | 505G(a)(3) | openfda.application_number | |
| brand name | Knee Pain Relief Gel-Patch | openfda.brand_name | |
| generic name | LIDOCAINE AND MENTHOL | openfda.generic_name | |
| manufacturer name | Guangzhou Liuquanmiao Import & Export Trade Co., Ltd. | openfda.manufacturer_name | |
| ndc | package | 83602-178-25 | openfda.package_ndc |
| ndc | package | 83602-178-15 | openfda.package_ndc |
| ndc | package | 83602-178-13 | openfda.package_ndc |
| ndc | package | 83602-178-36 | openfda.package_ndc |
| ndc | package | 83602-178-16 | openfda.package_ndc |
| ndc | package | 83602-178-26 | openfda.package_ndc |
| ndc | package | 83602-178-12 | openfda.package_ndc |
| ndc | package | 83602-178-35 | openfda.package_ndc |
| ndc | product | 83602-178 | openfda.product_ndc |
| ndc11 | package | 83602017816 | derived:openfda.package_ndc |
| ndc11 | package | 83602017812 | derived:openfda.package_ndc |
| ndc11 | package | 83602017815 | derived:openfda.package_ndc |
| ndc11 | package | 83602017813 | derived:openfda.package_ndc |
| ndc11 | package | 83602017825 | derived:openfda.package_ndc |
| ndc11 | package | 83602017835 | derived:openfda.package_ndc |
| ndc11 | package | 83602017836 | derived:openfda.package_ndc |
| ndc11 | package | 83602017826 | derived:openfda.package_ndc |
| rxcui | 1249758 | openfda.rxcui | |
| spl id | 54071db0-8180-ffe6-e063-6394a90a8625 | id | |
| spl set id | 54071b61-6e69-03e3-e063-6394a90a42f0 | set_id | |
| unii | 98PI200987 | openfda.unii | |
| unii | L7T10EIP3A | 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.