warnings
Warnings
Moxe Hand Sanitizer Eucalyptus Mint
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
- Moxe Hand Sanitizer Eucalyptus Mint
- Generic name
- ALCOHOL
- Manufacturer
- Premark Health Science
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 21636fb2-0624-117e-e063-6394a90ab9eb
- SPL ID
- 3400f4c0-28cd-d1d0-e063-6294a90a4662
- Version
- 2
- Effective date
- 2025-04-30
- Source export date
- 2026-09-28
- Source partition
- 4
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:25:02
| 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 | M003 | openfda.application_number | |
| brand name | Moxe Hand Sanitizer Eucalyptus Mint | openfda.brand_name | |
| generic name | ALCOHOL | openfda.generic_name | |
| manufacturer name | Premark Health Science | openfda.manufacturer_name | |
| ndc | package | 84004-002-32 | openfda.package_ndc |
| ndc | product | 84004-002 | openfda.product_ndc |
| ndc11 | package | 84004000232 | derived:openfda.package_ndc |
| rxcui | 581662 | openfda.rxcui | |
| spl id | 3400f4c0-28cd-d1d0-e063-6294a90a4662 | id | |
| spl set id | 21636fb2-0624-117e-e063-6394a90ab9eb | set_id | |
| unii | 3K9958V90M | 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.