warnings
Warnings ■ For external use only. ■ Avoid contact with eyes. ■ Do not apply to open wounds. ■ STOP USE and ask a doctor 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
- bc58b347-a3cb-4b36-8041-62d948438a81
- SPL ID
- 364c6f8f-dca5-cf27-e063-6294a90a99e6
- Version
- 11
- Effective date
- 2025-05-29
- Source export date
- 2026-09-28
- Source partition
- 6
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:38:55
| 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 | 81507-002-05 | openfda.package_ndc |
| ndc | package | 81507-002-04 | openfda.package_ndc |
| ndc | package | 81507-002-02 | openfda.package_ndc |
| ndc | package | 81507-002-01 | openfda.package_ndc |
| ndc | package | 81507-002-06 | openfda.package_ndc |
| ndc | package | 81507-002-03 | openfda.package_ndc |
| ndc | product | 81507-002 | openfda.product_ndc |
| ndc11 | package | 81507000205 | derived:openfda.package_ndc |
| ndc11 | package | 81507000206 | derived:openfda.package_ndc |
| ndc11 | package | 81507000203 | derived:openfda.package_ndc |
| ndc11 | package | 81507000202 | derived:openfda.package_ndc |
| ndc11 | package | 81507000201 | derived:openfda.package_ndc |
| ndc11 | package | 81507000204 | derived:openfda.package_ndc |
| rxcui | 2531532 | openfda.rxcui | |
| rxcui | 2603409 | openfda.rxcui | |
| spl id | 364c6f8f-dca5-cf27-e063-6294a90a99e6 | id | |
| spl set id | bc58b347-a3cb-4b36-8041-62d948438a81 | 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.