warnings
For external use only
Sumifun 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
- Sumifun Lidocaine Pain Relief Gel-Patch
- Generic name
- LIDOCAINE
- Manufacturer
- Guangzhou Zhupuyou E-commerce Co., Ltd
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 3d7dc8cc-0680-d94d-e063-6394a90ac8e8
- SPL ID
- 3d7dc8cc-0681-d94d-e063-6394a90ac8e8
- Version
- 1
- Effective date
- 2025-08-29
- 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 06:29:29
| 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 | Sumifun Lidocaine Pain Relief Gel-Patch | openfda.brand_name | |
| generic name | LIDOCAINE | openfda.generic_name | |
| manufacturer name | Guangzhou Zhupuyou E-commerce Co., Ltd | openfda.manufacturer_name | |
| ndc | package | 84165-016-34 | openfda.package_ndc |
| ndc | package | 84165-016-55 | openfda.package_ndc |
| ndc | package | 84165-016-35 | openfda.package_ndc |
| ndc | package | 84165-016-28 | openfda.package_ndc |
| ndc | package | 84165-016-53 | openfda.package_ndc |
| ndc | package | 84165-016-60 | openfda.package_ndc |
| ndc | package | 84165-016-08 | openfda.package_ndc |
| ndc | package | 84165-016-58 | openfda.package_ndc |
| ndc | package | 84165-016-30 | openfda.package_ndc |
| ndc | package | 84165-016-04 | openfda.package_ndc |
| ndc | package | 84165-016-45 | openfda.package_ndc |
| ndc | package | 84165-016-59 | openfda.package_ndc |
| ndc | package | 84165-016-43 | openfda.package_ndc |
| ndc | package | 84165-016-41 | openfda.package_ndc |
| ndc | package | 84165-016-22 | openfda.package_ndc |
| ndc | package | 84165-016-52 | openfda.package_ndc |
| ndc | package | 84165-016-29 | openfda.package_ndc |
| ndc | package | 84165-016-26 | openfda.package_ndc |
| ndc | package | 84165-016-50 | openfda.package_ndc |
| ndc | package | 84165-016-27 | openfda.package_ndc |
| ndc | package | 84165-016-13 | openfda.package_ndc |
| ndc | package | 84165-016-03 | openfda.package_ndc |
| ndc | package | 84165-016-54 | openfda.package_ndc |
| ndc | package | 84165-016-21 | openfda.package_ndc |
| ndc | package | 84165-016-18 | openfda.package_ndc |
| ndc | package | 84165-016-25 | openfda.package_ndc |
| ndc | package | 84165-016-48 | openfda.package_ndc |
| ndc | package | 84165-016-17 | openfda.package_ndc |
| ndc | package | 84165-016-56 | openfda.package_ndc |
| ndc | package | 84165-016-07 | openfda.package_ndc |
| ndc | package | 84165-016-40 | openfda.package_ndc |
| ndc | package | 84165-016-06 | openfda.package_ndc |
| ndc | package | 84165-016-10 | openfda.package_ndc |
| ndc | package | 84165-016-24 | openfda.package_ndc |
| ndc | package | 84165-016-20 | openfda.package_ndc |
| ndc | package | 84165-016-23 | 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.