warnings
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 AND MENTHOL
- Manufacturer
- Guangzhou Liuquanmiao Import & Export Trade Co., Ltd.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 49bcdf68-d8f4-64d8-e063-6394a90a9717
- SPL ID
- 56b7cbd0-2ef8-bcf1-e063-6394a90a7b26
- Version
- 4
- Effective date
- 2026-07-16
- Source export date
- 2026-09-28
- Source partition
- 8
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:56:26
| 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 | Lidocaine 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 | 83602-175-25 | openfda.package_ndc |
| ndc | package | 83602-175-11 | openfda.package_ndc |
| ndc | package | 83602-175-13 | openfda.package_ndc |
| ndc | package | 83602-175-05 | openfda.package_ndc |
| ndc | package | 83602-175-26 | openfda.package_ndc |
| ndc | package | 83602-175-07 | openfda.package_ndc |
| ndc | package | 83602-175-06 | openfda.package_ndc |
| ndc | package | 83602-175-24 | openfda.package_ndc |
| ndc | package | 83602-175-17 | openfda.package_ndc |
| ndc | package | 83602-175-12 | openfda.package_ndc |
| ndc | package | 83602-175-14 | openfda.package_ndc |
| ndc | package | 83602-175-18 | openfda.package_ndc |
| ndc | package | 83602-175-19 | openfda.package_ndc |
| ndc | package | 83602-175-08 | openfda.package_ndc |
| ndc | package | 83602-175-20 | openfda.package_ndc |
| ndc | package | 83602-175-01 | openfda.package_ndc |
| ndc | package | 83602-175-23 | openfda.package_ndc |
| ndc | product | 83602-175 | openfda.product_ndc |
| ndc11 | package | 83602017511 | derived:openfda.package_ndc |
| ndc11 | package | 83602017513 | derived:openfda.package_ndc |
| ndc11 | package | 83602017519 | derived:openfda.package_ndc |
| ndc11 | package | 83602017517 | derived:openfda.package_ndc |
| ndc11 | package | 83602017523 | derived:openfda.package_ndc |
| ndc11 | package | 83602017518 | derived:openfda.package_ndc |
| ndc11 | package | 83602017501 | derived:openfda.package_ndc |
| ndc11 | package | 83602017506 | derived:openfda.package_ndc |
| ndc11 | package | 83602017526 | derived:openfda.package_ndc |
| ndc11 | package | 83602017525 | derived:openfda.package_ndc |
| ndc11 | package | 83602017512 | derived:openfda.package_ndc |
| ndc11 | package | 83602017520 | derived:openfda.package_ndc |
| ndc11 | package | 83602017514 | derived:openfda.package_ndc |
| ndc11 | package | 83602017507 | derived:openfda.package_ndc |
| ndc11 | package | 83602017505 | derived:openfda.package_ndc |
| ndc11 | package | 83602017524 | derived:openfda.package_ndc |
| ndc11 | package | 83602017508 | derived:openfda.package_ndc |
| rxcui | 1249758 | openfda.rxcui |
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.