warnings
For external use only
Sumifun PLANTAR RELIEF ROLL -ON
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 PLANTAR RELIEF ROLL -ON
- Generic name
- 4% LIDOCAINE, 1% MENTHOL
- Manufacturer
- Guangzhou Zhupuyou E-commerce Co., Ltd
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 3c9ee60b-548a-979f-e063-6394a90a70b0
- SPL ID
- 3df16a4f-43c9-d73e-e063-6394a90ae436
- Version
- 2
- Effective date
- 2025-09-03
- Source export date
- 2026-09-28
- Source partition
- 11
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:18:50
| 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 PLANTAR RELIEF ROLL -ON | openfda.brand_name | |
| generic name | 4% LIDOCAINE, 1% MENTHOL | openfda.generic_name | |
| manufacturer name | Guangzhou Zhupuyou E-commerce Co., Ltd | openfda.manufacturer_name | |
| ndc | package | 84165-015-09 | openfda.package_ndc |
| ndc | package | 84165-015-08 | openfda.package_ndc |
| ndc | package | 84165-015-06 | openfda.package_ndc |
| ndc | package | 84165-015-03 | openfda.package_ndc |
| ndc | package | 84165-015-01 | openfda.package_ndc |
| ndc | package | 84165-015-10 | openfda.package_ndc |
| ndc | package | 84165-015-05 | openfda.package_ndc |
| ndc | package | 84165-015-07 | openfda.package_ndc |
| ndc | package | 84165-015-02 | openfda.package_ndc |
| ndc | package | 84165-015-04 | openfda.package_ndc |
| ndc | product | 84165-015 | openfda.product_ndc |
| ndc11 | package | 84165001503 | derived:openfda.package_ndc |
| ndc11 | package | 84165001506 | derived:openfda.package_ndc |
| ndc11 | package | 84165001507 | derived:openfda.package_ndc |
| ndc11 | package | 84165001502 | derived:openfda.package_ndc |
| ndc11 | package | 84165001510 | derived:openfda.package_ndc |
| ndc11 | package | 84165001504 | derived:openfda.package_ndc |
| ndc11 | package | 84165001505 | derived:openfda.package_ndc |
| ndc11 | package | 84165001508 | derived:openfda.package_ndc |
| ndc11 | package | 84165001509 | derived:openfda.package_ndc |
| ndc11 | package | 84165001501 | derived:openfda.package_ndc |
| rxcui | 1804176 | openfda.rxcui | |
| spl id | 3df16a4f-43c9-d73e-e063-6394a90ae436 | id | |
| spl set id | 3c9ee60b-548a-979f-e063-6394a90a70b0 | set_id | |
| unii | 98PI200987 | openfda.unii | |
| unii | L7T10EIP3A | openfda.unii |
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.