warnings
Warnings: For external use only
Eucamint
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
- Eucamint
- Generic name
- MENTHOL, CAMPHOR
- Manufacturer
- Indiana Botanic Gardens
- Product type
- HUMAN OTC DRUG
- SPL set ID
- d79bc8de-9efb-4996-a55c-accda0f8edb2
- SPL ID
- 586256ec-2a26-89a5-e063-6394a90a40df
- Version
- 5
- Effective date
- 2026-08-06
- Source export date
- 2026-10-27
- Source partition
- 2
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-27/29a1aba6a935d72bab5474118c2ccf25cb52dfe8488fe1593c734ea6c04e3722/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 19:45:43
| 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 | M012 | openfda.application_number | |
| brand name | Eucamint | openfda.brand_name | |
| generic name | MENTHOL, CAMPHOR | openfda.generic_name | |
| manufacturer name | Indiana Botanic Gardens | openfda.manufacturer_name | |
| ndc | package | 10578-001-04 | openfda.package_ndc |
| ndc | package | 10578-001-02 | openfda.package_ndc |
| ndc | product | 10578-001 | openfda.product_ndc |
| ndc11 | package | 10578000104 | derived:openfda.package_ndc |
| ndc11 | package | 10578000102 | derived:openfda.package_ndc |
| rxcui | 1663854 | openfda.rxcui | |
| rxcui | 1663849 | openfda.rxcui | |
| spl id | 586256ec-2a26-89a5-e063-6394a90a40df | id | |
| spl set id | d79bc8de-9efb-4996-a55c-accda0f8edb2 | set_id | |
| unii | L7T10EIP3A | openfda.unii | |
| unii | 5TJD82A1ET | 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.