warnings
For external use only
Cold Hot Chinese Red Tiger Pain Relief Gel 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
- Cold Hot Chinese Red Tiger Pain Relief Gel Roll-On
- Generic name
- MENTHOL
- Manufacturer
- Guangzhou Zhupuyou E-commerce Co., Ltd
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 352798e1-1e09-3d47-e063-6394a90ad404
- SPL ID
- 352798e1-1e0a-3d47-e063-6394a90ad404
- Version
- 1
- Effective date
- 2025-05-15
- Source export date
- 2026-09-28
- Source partition
- 7
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:45:44
| 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 Gel Roll-On | openfda.brand_name | |
| generic name | MENTHOL | openfda.generic_name | |
| manufacturer name | Guangzhou Zhupuyou E-commerce Co., Ltd | openfda.manufacturer_name | |
| ndc | package | 84165-008-04 | openfda.package_ndc |
| ndc | package | 84165-008-07 | openfda.package_ndc |
| ndc | package | 84165-008-06 | openfda.package_ndc |
| ndc | package | 84165-008-08 | openfda.package_ndc |
| ndc | package | 84165-008-02 | openfda.package_ndc |
| ndc | package | 84165-008-05 | openfda.package_ndc |
| ndc | package | 84165-008-03 | openfda.package_ndc |
| ndc | package | 84165-008-01 | openfda.package_ndc |
| ndc | package | 84165-008-10 | openfda.package_ndc |
| ndc | package | 84165-008-09 | openfda.package_ndc |
| ndc | product | 84165-008 | openfda.product_ndc |
| ndc11 | package | 84165000807 | derived:openfda.package_ndc |
| ndc11 | package | 84165000805 | derived:openfda.package_ndc |
| ndc11 | package | 84165000801 | derived:openfda.package_ndc |
| ndc11 | package | 84165000802 | derived:openfda.package_ndc |
| ndc11 | package | 84165000803 | derived:openfda.package_ndc |
| ndc11 | package | 84165000804 | derived:openfda.package_ndc |
| ndc11 | package | 84165000808 | derived:openfda.package_ndc |
| ndc11 | package | 84165000810 | derived:openfda.package_ndc |
| ndc11 | package | 84165000809 | derived:openfda.package_ndc |
| ndc11 | package | 84165000806 | derived:openfda.package_ndc |
| rxcui | 415974 | openfda.rxcui | |
| spl id | 352798e1-1e0a-3d47-e063-6394a90ad404 | id | |
| spl set id | 352798e1-1e09-3d47-e063-6394a90ad404 | set_id | |
| 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.