warnings
Warnings For external use only
Alpet E2 Sanitizing Foam
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
- Alpet E2 Sanitizing Foam
- Generic name
- CHLOROXYLENOL
- Manufacturer
- Best Sanitizers, Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 5c7bdeb0-25e3-4e7a-8789-6b6fc6f32a31
- SPL ID
- 288e010d-ea76-ac1d-e063-6394a90aabb6
- Version
- 3
- Effective date
- 2024-12-05
- Source export date
- 2026-09-28
- Source partition
- 5
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:27:52
| 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 | 505G(a)(3) | openfda.application_number | |
| brand name | Alpet E2 Sanitizing Foam | openfda.brand_name | |
| generic name | CHLOROXYLENOL | openfda.generic_name | |
| manufacturer name | Best Sanitizers, Inc. | openfda.manufacturer_name | |
| ndc | package | 59900-208-01 | openfda.package_ndc |
| ndc | package | 59900-208-08 | openfda.package_ndc |
| ndc | package | 59900-208-05 | openfda.package_ndc |
| ndc | package | 59900-208-03 | openfda.package_ndc |
| ndc | package | 59900-208-09 | openfda.package_ndc |
| ndc | package | 59900-208-04 | openfda.package_ndc |
| ndc | package | 59900-208-06 | openfda.package_ndc |
| ndc | package | 59900-208-07 | openfda.package_ndc |
| ndc | package | 59900-208-02 | openfda.package_ndc |
| ndc | product | 59900-208 | openfda.product_ndc |
| ndc11 | package | 59900020807 | derived:openfda.package_ndc |
| ndc11 | package | 59900020804 | derived:openfda.package_ndc |
| ndc11 | package | 59900020808 | derived:openfda.package_ndc |
| ndc11 | package | 59900020802 | derived:openfda.package_ndc |
| ndc11 | package | 59900020803 | derived:openfda.package_ndc |
| ndc11 | package | 59900020801 | derived:openfda.package_ndc |
| ndc11 | package | 59900020809 | derived:openfda.package_ndc |
| ndc11 | package | 59900020806 | derived:openfda.package_ndc |
| ndc11 | package | 59900020805 | derived:openfda.package_ndc |
| rxcui | 1043129 | openfda.rxcui | |
| spl id | 288e010d-ea76-ac1d-e063-6394a90aabb6 | id | |
| spl set id | 5c7bdeb0-25e3-4e7a-8789-6b6fc6f32a31 | set_id | |
| unii | 0F32U78V2Q | 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.