warnings
For external use only
Chinese Red Tiger Lidocaine Patches
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
- Chinese Red Tiger Lidocaine Patches
- Generic name
- LIDOCAINE
- Manufacturer
- Guangzhou Zhupuyou E-commerce Co., Ltd
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 20cd369c-3e98-3d8f-e063-6394a90a0824
- SPL ID
- 3c0e024c-0c59-88b8-e063-6394a90acce3
- Version
- 8
- Effective date
- 2025-08-10
- Source export date
- 2026-09-28
- Source partition
- 5
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:34:00
| 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 | Chinese Red Tiger Lidocaine Patches | openfda.brand_name | |
| generic name | LIDOCAINE | openfda.generic_name | |
| manufacturer name | Guangzhou Zhupuyou E-commerce Co., Ltd | openfda.manufacturer_name | |
| ndc | package | 84165-102-30 | openfda.package_ndc |
| ndc | package | 84165-102-58 | openfda.package_ndc |
| ndc | package | 84165-102-06 | openfda.package_ndc |
| ndc | package | 84165-102-50 | openfda.package_ndc |
| ndc | package | 84165-102-19 | openfda.package_ndc |
| ndc | package | 84165-102-54 | openfda.package_ndc |
| ndc | package | 84165-102-57 | openfda.package_ndc |
| ndc | package | 84165-102-18 | openfda.package_ndc |
| ndc | package | 84165-102-55 | openfda.package_ndc |
| ndc | package | 84165-102-10 | openfda.package_ndc |
| ndc | package | 84165-102-09 | openfda.package_ndc |
| ndc | package | 84165-102-46 | openfda.package_ndc |
| ndc | package | 84165-102-59 | openfda.package_ndc |
| ndc | package | 84165-102-25 | openfda.package_ndc |
| ndc | package | 84165-102-48 | openfda.package_ndc |
| ndc | package | 84165-102-38 | openfda.package_ndc |
| ndc | package | 84165-102-08 | openfda.package_ndc |
| ndc | package | 84165-102-49 | openfda.package_ndc |
| ndc | package | 84165-102-36 | openfda.package_ndc |
| ndc | package | 84165-102-51 | openfda.package_ndc |
| ndc | package | 84165-102-31 | openfda.package_ndc |
| ndc | package | 84165-102-47 | openfda.package_ndc |
| ndc | package | 84165-102-07 | openfda.package_ndc |
| ndc | package | 84165-102-43 | openfda.package_ndc |
| ndc | package | 84165-102-20 | openfda.package_ndc |
| ndc | package | 84165-102-35 | openfda.package_ndc |
| ndc | package | 84165-102-12 | openfda.package_ndc |
| ndc | package | 84165-102-21 | openfda.package_ndc |
| ndc | package | 84165-102-52 | openfda.package_ndc |
| ndc | package | 84165-102-53 | openfda.package_ndc |
| ndc | package | 84165-102-17 | openfda.package_ndc |
| ndc | package | 84165-102-42 | openfda.package_ndc |
| ndc | package | 84165-102-05 | openfda.package_ndc |
| ndc | package | 84165-102-28 | openfda.package_ndc |
| ndc | package | 84165-102-32 | openfda.package_ndc |
| ndc | package | 84165-102-15 | 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.