warnings
For external use only
LIDOCAINE PAIN RELIEVING 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 RELIEVING Gel-Patch
- Generic name
- LIDOCAINE
- Manufacturer
- Guangzhou Zhupuyou E-commerce Co., Ltd
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 2159fb73-cf6c-184a-e063-6394a90a1d14
- SPL ID
- 47db760e-46e8-2938-e063-6394a90a0afb
- Version
- 3
- Effective date
- 2026-01-08
- Source export date
- 2026-09-28
- Source partition
- 6
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:35:07
| 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 RELIEVING Gel-Patch | openfda.brand_name | |
| generic name | LIDOCAINE | openfda.generic_name | |
| manufacturer name | Guangzhou Zhupuyou E-commerce Co., Ltd | openfda.manufacturer_name | |
| ndc | package | 84165-103-29 | openfda.package_ndc |
| ndc | package | 84165-103-50 | openfda.package_ndc |
| ndc | package | 84165-103-11 | openfda.package_ndc |
| ndc | package | 84165-103-01 | openfda.package_ndc |
| ndc | package | 84165-103-20 | openfda.package_ndc |
| ndc | package | 84165-103-56 | openfda.package_ndc |
| ndc | package | 84165-103-18 | openfda.package_ndc |
| ndc | package | 84165-103-52 | openfda.package_ndc |
| ndc | package | 84165-103-15 | openfda.package_ndc |
| ndc | package | 84165-103-08 | openfda.package_ndc |
| ndc | package | 84165-103-26 | openfda.package_ndc |
| ndc | package | 84165-103-13 | openfda.package_ndc |
| ndc | package | 84165-103-16 | openfda.package_ndc |
| ndc | package | 84165-103-38 | openfda.package_ndc |
| ndc | package | 84165-103-47 | openfda.package_ndc |
| ndc | package | 84165-103-42 | openfda.package_ndc |
| ndc | package | 84165-103-49 | openfda.package_ndc |
| ndc | package | 84165-103-12 | openfda.package_ndc |
| ndc | package | 84165-103-41 | openfda.package_ndc |
| ndc | package | 84165-103-23 | openfda.package_ndc |
| ndc | package | 84165-103-36 | openfda.package_ndc |
| ndc | package | 84165-103-45 | openfda.package_ndc |
| ndc | package | 84165-103-30 | openfda.package_ndc |
| ndc | package | 84165-103-34 | openfda.package_ndc |
| ndc | package | 84165-103-35 | openfda.package_ndc |
| ndc | package | 84165-103-40 | openfda.package_ndc |
| ndc | package | 84165-103-06 | openfda.package_ndc |
| ndc | package | 84165-103-05 | openfda.package_ndc |
| ndc | package | 84165-103-27 | openfda.package_ndc |
| ndc | package | 84165-103-09 | openfda.package_ndc |
| ndc | package | 84165-103-07 | openfda.package_ndc |
| ndc | package | 84165-103-31 | openfda.package_ndc |
| ndc | package | 84165-103-10 | openfda.package_ndc |
| ndc | package | 84165-103-53 | openfda.package_ndc |
| ndc | package | 84165-103-17 | openfda.package_ndc |
| ndc | package | 84165-103-55 | 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.