warnings
For external use only
COLD HOT CHINESE RED TIGER PAIN RELIEF GeI-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
- COLD HOT CHINESE RED TIGER PAIN RELIEF GeI-Patch
- Generic name
- MENTHOL
- Manufacturer
- Guangzhou Zhupuyou E-commerce Co., Ltd
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 32b7d73c-a191-7843-e063-6394a90aa631
- SPL ID
- 32b7d73c-a192-7843-e063-6394a90aa631
- Version
- 1
- Effective date
- 2025-04-14
- Source export date
- 2026-09-28
- Source partition
- 1
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/9c7783846d422acb0c9e59457606951c785a7d28cc631c8cc4839d0dc7c55f39/drug-label-0001-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:14:30
| 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 | COLD HOT CHINESE RED TIGER PAIN RELIEF GeI-Patch | openfda.brand_name | |
| generic name | MENTHOL | openfda.generic_name | |
| manufacturer name | Guangzhou Zhupuyou E-commerce Co., Ltd | openfda.manufacturer_name | |
| ndc | package | 84165-004-18 | openfda.package_ndc |
| ndc | package | 84165-004-05 | openfda.package_ndc |
| ndc | package | 84165-004-32 | openfda.package_ndc |
| ndc | package | 84165-004-28 | openfda.package_ndc |
| ndc | package | 84165-004-08 | openfda.package_ndc |
| ndc | package | 84165-004-01 | openfda.package_ndc |
| ndc | package | 84165-004-10 | openfda.package_ndc |
| ndc | package | 84165-004-37 | openfda.package_ndc |
| ndc | package | 84165-004-55 | openfda.package_ndc |
| ndc | package | 84165-004-54 | openfda.package_ndc |
| ndc | package | 84165-004-53 | openfda.package_ndc |
| ndc | package | 84165-004-19 | openfda.package_ndc |
| ndc | package | 84165-004-29 | openfda.package_ndc |
| ndc | package | 84165-004-24 | openfda.package_ndc |
| ndc | package | 84165-004-25 | openfda.package_ndc |
| ndc | package | 84165-004-49 | openfda.package_ndc |
| ndc | package | 84165-004-13 | openfda.package_ndc |
| ndc | package | 84165-004-46 | openfda.package_ndc |
| ndc | package | 84165-004-11 | openfda.package_ndc |
| ndc | package | 84165-004-27 | openfda.package_ndc |
| ndc | package | 84165-004-48 | openfda.package_ndc |
| ndc | package | 84165-004-15 | openfda.package_ndc |
| ndc | package | 84165-004-30 | openfda.package_ndc |
| ndc | package | 84165-004-51 | openfda.package_ndc |
| ndc | package | 84165-004-35 | openfda.package_ndc |
| ndc | package | 84165-004-21 | openfda.package_ndc |
| ndc | package | 84165-004-26 | openfda.package_ndc |
| ndc | package | 84165-004-22 | openfda.package_ndc |
| ndc | package | 84165-004-06 | openfda.package_ndc |
| ndc | package | 84165-004-31 | openfda.package_ndc |
| ndc | package | 84165-004-14 | openfda.package_ndc |
| ndc | package | 84165-004-38 | openfda.package_ndc |
| ndc | package | 84165-004-39 | openfda.package_ndc |
| ndc | package | 84165-004-23 | openfda.package_ndc |
| ndc | package | 84165-004-16 | openfda.package_ndc |
| ndc | package | 84165-004-09 | 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.