warnings
Warnings For external use only. Do not use on broken or irritated skin Ask a doctor before use if you have kidney disease.
Hand Antiperspirant Nightly Use
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
- Hand Antiperspirant Nightly Use
- Generic name
- ALUMINUM CHLORIDE HEXAHYDRATE
- Manufacturer
- Clutch Inc
- Product type
- HUMAN OTC DRUG
- SPL set ID
- a70d9eff-b5a3-5c52-e053-2a95a90a704c
- SPL ID
- 597f62e0-ff43-5739-e063-6394a90a9c5a
- Version
- 3
- Effective date
- 2026-08-20
- Source export date
- 2026-11-06
- Source partition
- 2
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-11-06/4dafeb36642dffb72e2138939a956de402f722ea8c14c08cd87068efd3669f01/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
- Import run
- 20261108T063105Z
- Imported at
- 2026-11-08 06:49:28
| 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 | Hand Antiperspirant Nightly Use | openfda.brand_name | |
| generic name | ALUMINUM CHLORIDE HEXAHYDRATE | openfda.generic_name | |
| manufacturer name | Clutch Inc | openfda.manufacturer_name | |
| ndc | package | 74307-008-01 | openfda.package_ndc |
| ndc | product | 74307-008 | openfda.product_ndc |
| ndc11 | package | 74307000801 | derived:openfda.package_ndc |
| spl id | 597f62e0-ff43-5739-e063-6394a90a9c5a | id | |
| spl set id | a70d9eff-b5a3-5c52-e053-2a95a90a704c | set_id | |
| unii | 3CYT62D3GA | 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.