warnings
Warnings For external use only. Do not use on broken skin. Ask a doctor before use if you have kidney disease. Stop use if rash or irritation occurs.
Degree Men Motionsense UltraClear Black and White 48H Antiperspirant
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
- Degree Men Motionsense UltraClear Black and White 48H Antiperspirant
- Generic name
- ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY
- Manufacturer
- Conopco, Inc. d/b/a Unilever
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 056f3511-5f92-4cb8-8188-88e8525ae392
- SPL ID
- 253e0b71-d718-c9b5-e063-6394a90a57b5
- Version
- 5
- Effective date
- 2024-10-24
- Source export date
- 2026-10-12
- Source partition
- 12
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/edd23646015c9adc800cdbe2b778398a2d2b70e90dce5721ef2b191499a0397f/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:52:31
| 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 | Degree Men Motionsense UltraClear Black and White 48H Antiperspirant | openfda.brand_name | |
| generic name | ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY | openfda.generic_name | |
| manufacturer name | Conopco, Inc. d/b/a Unilever | openfda.manufacturer_name | |
| ndc | package | 64942-1466-3 | openfda.package_ndc |
| ndc | package | 64942-1466-1 | openfda.package_ndc |
| ndc | package | 64942-1466-2 | openfda.package_ndc |
| ndc | product | 64942-1466 | openfda.product_ndc |
| ndc11 | package | 64942146603 | derived:openfda.package_ndc |
| ndc11 | package | 64942146601 | derived:openfda.package_ndc |
| ndc11 | package | 64942146602 | derived:openfda.package_ndc |
| spl id | 253e0b71-d718-c9b5-e063-6394a90a57b5 | id | |
| spl set id | 056f3511-5f92-4cb8-8188-88e8525ae392 | set_id | |
| unii | 8O386558JE | 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.