warnings
For external use only
myDerm Cooling Menthol Pain Relief with 50 Percent More Menthol
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
- myDerm Cooling Menthol Pain Relief with 50 Percent More Menthol
- Generic name
- MENTHOL
- Manufacturer
- Inspec Solutions LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- d4276749-eeff-28f7-e053-2a95a90a593d
- SPL ID
- 2d047890-53dd-a24e-e063-6294a90a2b12
- Version
- 5
- Effective date
- 2025-01-31
- Source export date
- 2026-10-30
- 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/2026-10-30/a3e33fe073aa0aa94eb690c6684c74434c63cebfbf7c5530205a2c3e957ecb8b/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
- Import run
- 20261102T182004Z
- Imported at
- 2026-11-02 19:47:11
| 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 | myDerm Cooling Menthol Pain Relief with 50 Percent More Menthol | openfda.brand_name | |
| generic name | MENTHOL | openfda.generic_name | |
| manufacturer name | Inspec Solutions LLC | openfda.manufacturer_name | |
| ndc | package | 72667-020-01 | openfda.package_ndc |
| ndc | product | 72667-020 | openfda.product_ndc |
| ndc11 | package | 72667002001 | derived:openfda.package_ndc |
| spl id | 2d047890-53dd-a24e-e063-6294a90a2b12 | id | |
| spl set id | d4276749-eeff-28f7-e053-2a95a90a593d | 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.