warnings
Warnings For external use only Allergy alert: Do not use if you are allergic to capsicum, chili peppers, or any ingredients in this product.
Coralite Pain Relief Hot
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
- Coralite Pain Relief Hot
- Generic name
- MENTHOL AND CAPSAICIN
- Manufacturer
- United Exchange Corporation
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 78eb133d-01bb-6466-e053-2991aa0accc0
- SPL ID
- 41dc963f-67e2-e705-e063-6394a90a2b96
- Version
- 5
- Effective date
- 2025-10-23
- Source export date
- 2026-10-27
- Source partition
- 14
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-27/9122bd1bdced046e8f62ea012d80757473b7d83ea1faeea61faef490e06fd630/drug-label-0014-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 21:09:58
| 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 | Coralite Pain Relief Hot | openfda.brand_name | |
| generic name | MENTHOL AND CAPSAICIN | openfda.generic_name | |
| manufacturer name | United Exchange Corporation | openfda.manufacturer_name | |
| ndc | package | 65923-146-02 | openfda.package_ndc |
| ndc | product | 65923-146 | openfda.product_ndc |
| ndc11 | package | 65923014602 | derived:openfda.package_ndc |
| rxcui | 1484488 | openfda.rxcui | |
| spl id | 41dc963f-67e2-e705-e063-6394a90a2b96 | id | |
| spl set id | 78eb133d-01bb-6466-e053-2991aa0accc0 | set_id | |
| unii | S07O44R1ZM | 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.