warnings
For external use only. Do not use on broken skin. Stop use if rash or irritation occurs. Ask a doctor before use if you have kidney disease.
Dove
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
- Dove
- Generic name
- MEN CARE SANDALWOOD AMBER 72H ANTIPERSPIRANT
- Manufacturer
- Conopco d/b/a/ Unilever
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 31ab1018-d5e3-ab12-e063-6394a90a1e88
- SPL ID
- 31ab1018-d5e4-ab12-e063-6394a90a1e88
- Version
- 1
- Effective date
- 2025-03-31
- Source export date
- 2026-11-06
- 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/2026-11-06/7dfa569f2d8f065241260fd9a4886d0ef0a3120fd6ee31d6d07c234e689e8c91/drug-label-0004-of-0014.json.zip
- Source manifest SHA-256
- 8dff71fbef1291eb7711013e9a3a06194930757924a8946ae3034107a98d9463
- Import run
- 20261106T075659Z
- Imported at
- 2026-11-06 08:21:18
| 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 | M019 | openfda.application_number | |
| brand name | Dove | openfda.brand_name | |
| generic name | MEN CARE SANDALWOOD AMBER 72H ANTIPERSPIRANT | openfda.generic_name | |
| manufacturer name | Conopco d/b/a/ Unilever | openfda.manufacturer_name | |
| ndc | package | 64942-2359-1 | openfda.package_ndc |
| ndc | product | 64942-2359 | openfda.product_ndc |
| ndc11 | package | 64942235901 | derived:openfda.package_ndc |
| spl id | 31ab1018-d5e4-ab12-e063-6394a90a1e88 | id | |
| spl set id | 31ab1018-d5e3-ab12-e063-6394a90a1e88 | set_id | |
| unii | UCN889409V | 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.