warnings
Warnings For external use only
Ban Roll-On Antiperspirant Deodorant Unscented
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
- Ban Roll-On Antiperspirant Deodorant Unscented
- Generic name
- ALUMINUM CHLOROHYDRATE
- Manufacturer
- Kao USA Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 57a3d112-3f8e-4d23-864f-d834bcf25385
- SPL ID
- 2b205b12-5946-161f-e063-6394a90a5a66
- Version
- 14
- Effective date
- 2025-01-01
- Source export date
- 2026-10-12
- Source partition
- 9
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/fb14b8f3d34b45230a84f851c029385f512adf3f002423a9b78d4f7ca626ecec/drug-label-0009-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:26:02
| 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 | Ban Roll-On Antiperspirant Deodorant Unscented | openfda.brand_name | |
| generic name | ALUMINUM CHLOROHYDRATE | openfda.generic_name | |
| manufacturer name | Kao USA Inc. | openfda.manufacturer_name | |
| ndc | package | 10596-338-15 | openfda.package_ndc |
| ndc | package | 10596-338-11 | openfda.package_ndc |
| ndc | package | 10596-338-70 | openfda.package_ndc |
| ndc | package | 10596-338-35 | openfda.package_ndc |
| ndc | package | 10596-338-14 | openfda.package_ndc |
| ndc | product | 10596-338 | openfda.product_ndc |
| ndc11 | package | 10596033835 | derived:openfda.package_ndc |
| ndc11 | package | 10596033870 | derived:openfda.package_ndc |
| ndc11 | package | 10596033811 | derived:openfda.package_ndc |
| ndc11 | package | 10596033814 | derived:openfda.package_ndc |
| ndc11 | package | 10596033815 | derived:openfda.package_ndc |
| spl id | 2b205b12-5946-161f-e063-6394a90a5a66 | id | |
| spl set id | 57a3d112-3f8e-4d23-864f-d834bcf25385 | set_id | |
| unii | HPN8MZW13M | 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.