warnings
Warnings FOR EXTERNAL USE ONLY, provides penetrating pain relief
Cannarelief 1000mg
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
- Cannarelief 1000mg
- Generic name
- MENTHOL
- Manufacturer
- Carolina Cannabis Creations LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 01e2ae1a-c969-6dd2-e063-6394a90a9d9e
- SPL ID
- 2bca4263-a06f-45ee-e063-6394a90a48f5
- Version
- 2
- Effective date
- 2025-01-15
- Source export date
- 2026-10-27
- 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/2026-10-27/977776a6cc37ec1c77259da8a93ae161850a3aa120341096e5a03428b84d016b/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 20:57:35
| 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 | Cannarelief 1000mg | openfda.brand_name | |
| generic name | MENTHOL | openfda.generic_name | |
| manufacturer name | Carolina Cannabis Creations LLC | openfda.manufacturer_name | |
| ndc | package | 82876-010-49 | openfda.package_ndc |
| ndc | product | 82876-010 | openfda.product_ndc |
| ndc11 | package | 82876001049 | derived:openfda.package_ndc |
| spl id | 2bca4263-a06f-45ee-e063-6394a90a48f5 | id | |
| spl set id | 01e2ae1a-c969-6dd2-e063-6394a90a9d9e | 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.