warnings
Warnings For external use only
Ban Roll-On Antiperspirant Deodorant Powder Fresh
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 Powder Fresh
- Generic name
- ALUMINUM CHLOROHYDRATE
- Manufacturer
- Kao USA Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- b99e8972-24e6-4f01-80f5-d071bbab8d30
- SPL ID
- 23fbdedd-afae-e476-e063-6294a90ac410
- Version
- 10
- Effective date
- 2024-10-08
- Source export date
- 2026-08-01
- Source partition
- 11
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-08-01/8ac060fefb6f4d67c41cc2c9e4330286ca93c48094c18386c11bf706a1d8bd34/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
- Import run
- 20260801T225920Z
- Imported at
- 2026-08-01 23:27:16
| 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 Powder Fresh | openfda.brand_name | |
| generic name | ALUMINUM CHLOROHYDRATE | openfda.generic_name | |
| manufacturer name | Kao USA Inc. | openfda.manufacturer_name | |
| ndc | package | 10596-337-35 | openfda.package_ndc |
| ndc | package | 10596-337-14 | openfda.package_ndc |
| ndc | package | 10596-337-15 | openfda.package_ndc |
| ndc | package | 10596-337-70 | openfda.package_ndc |
| ndc | product | 10596-337 | openfda.product_ndc |
| ndc11 | package | 10596033714 | derived:openfda.package_ndc |
| ndc11 | package | 10596033735 | derived:openfda.package_ndc |
| ndc11 | package | 10596033770 | derived:openfda.package_ndc |
| ndc11 | package | 10596033715 | derived:openfda.package_ndc |
| spl id | 23fbdedd-afae-e476-e063-6294a90ac410 | id | |
| spl set id | b99e8972-24e6-4f01-80f5-d071bbab8d30 | set_id | |
| unii | HPN8MZW13M | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.