warnings
Warnings ■ For external use only. ■ Avoid contact with eyes. ■ Do not apply to open wounds. ■ STOP USE and ask a physician if condition worsens or symptoms persist for more than seven days. ■ Keep out of reach of children.
Dermeleve
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
- Dermeleve
- Generic name
- ALUMINUM ACETATE
- Manufacturer
- Advanced Derm Solutions LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 5dd4c952-8880-4c06-9c09-20c6a3cdd0f5
- SPL ID
- 364c7a24-4e3f-c622-e063-6394a90a3a8f
- Version
- 7
- Effective date
- 2025-05-29
- 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 05:33:51
| 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 | M016 | openfda.application_number | |
| brand name | Dermeleve | openfda.brand_name | |
| generic name | ALUMINUM ACETATE | openfda.generic_name | |
| manufacturer name | Advanced Derm Solutions LLC | openfda.manufacturer_name | |
| ndc | package | 81507-003-01 | openfda.package_ndc |
| ndc | package | 81507-003-02 | openfda.package_ndc |
| ndc | product | 81507-003 | openfda.product_ndc |
| ndc11 | package | 81507000302 | derived:openfda.package_ndc |
| ndc11 | package | 81507000301 | derived:openfda.package_ndc |
| rxcui | 2531532 | openfda.rxcui | |
| rxcui | 2603409 | openfda.rxcui | |
| spl id | 364c7a24-4e3f-c622-e063-6394a90a3a8f | id | |
| spl set id | 5dd4c952-8880-4c06-9c09-20c6a3cdd0f5 | set_id | |
| unii | 80EHD8I43D | 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.