warnings
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 AND MENTHOL
- Manufacturer
- Guangzhou Liuquanmiao Import & Export Trade Co., Ltd.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 32e1df3a-2f8f-68df-e063-6294a90aa1d1
- SPL ID
- 520ef0b6-695c-d9b2-e063-6294a90ab81c
- Version
- 3
- Effective date
- 2026-05-17
- Source export date
- 2026-09-28
- Source partition
- 10
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:08:10
| 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 | 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 | 83602-172-37 | openfda.package_ndc |
| ndc | package | 83602-172-46 | openfda.package_ndc |
| ndc | package | 83602-172-17 | openfda.package_ndc |
| ndc | package | 83602-172-45 | openfda.package_ndc |
| ndc | package | 83602-172-24 | openfda.package_ndc |
| ndc | package | 83602-172-44 | openfda.package_ndc |
| ndc | package | 83602-172-32 | openfda.package_ndc |
| ndc | package | 83602-172-36 | openfda.package_ndc |
| ndc | package | 83602-172-13 | openfda.package_ndc |
| ndc | package | 83602-172-43 | openfda.package_ndc |
| ndc | package | 83602-172-42 | openfda.package_ndc |
| ndc | package | 83602-172-34 | openfda.package_ndc |
| ndc | package | 83602-172-40 | openfda.package_ndc |
| ndc | package | 83602-172-39 | openfda.package_ndc |
| ndc | package | 83602-172-27 | openfda.package_ndc |
| ndc | package | 83602-172-14 | openfda.package_ndc |
| ndc | package | 83602-172-23 | openfda.package_ndc |
| ndc | package | 83602-172-35 | openfda.package_ndc |
| ndc | package | 83602-172-33 | openfda.package_ndc |
| ndc | package | 83602-172-29 | openfda.package_ndc |
| ndc | package | 83602-172-38 | openfda.package_ndc |
| ndc | package | 83602-172-21 | openfda.package_ndc |
| ndc | package | 83602-172-26 | openfda.package_ndc |
| ndc | package | 83602-172-22 | openfda.package_ndc |
| ndc | package | 83602-172-20 | openfda.package_ndc |
| ndc | package | 83602-172-12 | openfda.package_ndc |
| ndc | package | 83602-172-41 | openfda.package_ndc |
| ndc | package | 83602-172-16 | openfda.package_ndc |
| ndc | package | 83602-172-30 | openfda.package_ndc |
| ndc | package | 83602-172-19 | openfda.package_ndc |
| ndc | product | 83602-172 | openfda.product_ndc |
| ndc11 | package | 83602017229 | derived:openfda.package_ndc |
| ndc11 | package | 83602017227 | derived:openfda.package_ndc |
| ndc11 | package | 83602017237 | derived:openfda.package_ndc |
| ndc11 | package | 83602017242 | derived:openfda.package_ndc |
| ndc11 | package | 83602017239 | derived: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.