warnings
Warnings
Degree
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
- Generic name
- ADVANCED COCONUT RUSH DRY SPRAY 72H ANTIPERSPIRANT DEODORANT
- Manufacturer
- Conopco, Inc. d/b/a Unilever
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 05165463-30eb-46cd-e063-6394a90a53e3
- SPL ID
- 264b34d9-e2cf-96ca-e063-6394a90a0b6f
- Version
- 2
- Effective date
- 2024-11-06
- Source export date
- 2026-11-06
- Source partition
- 1
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-11-06/d05434af5edc4383b7c7894a8f2d94df21171d17714450933cecdfc35cedfa3d/drug-label-0001-of-0014.json.zip
- Source manifest SHA-256
- 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
- Import run
- 20261108T063105Z
- Imported at
- 2026-11-08 06:46:34
| 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 | openfda.brand_name | |
| generic name | ADVANCED COCONUT RUSH DRY SPRAY 72H ANTIPERSPIRANT DEODORANT | openfda.generic_name | |
| manufacturer name | Conopco, Inc. d/b/a Unilever | openfda.manufacturer_name | |
| ndc | package | 64942-2202-1 | openfda.package_ndc |
| ndc | product | 64942-2202 | openfda.product_ndc |
| ndc11 | package | 64942220201 | derived:openfda.package_ndc |
| spl id | 264b34d9-e2cf-96ca-e063-6394a90a0b6f | id | |
| spl set id | 05165463-30eb-46cd-e063-6394a90a53e3 | 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.