warnings
Warnings For external use only. Do not use on broken skin
Underarm Antiperspirant Daily Use Fresh Linen Scent
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
- Underarm Antiperspirant Daily Use Fresh Linen Scent
- Generic name
- ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY
- Manufacturer
- Clutch Inc
- Product type
- HUMAN OTC DRUG
- SPL set ID
- ceb71229-6c26-7ebf-e053-2a95a90ae8ad
- SPL ID
- 598025f7-a379-6780-e063-6294a90a40a0
- Version
- 5
- Effective date
- 2026-08-20
- Source export date
- 2026-09-28
- 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/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:28:28
| 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 | Underarm Antiperspirant Daily Use Fresh Linen Scent | openfda.brand_name | |
| generic name | ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY | openfda.generic_name | |
| manufacturer name | Clutch Inc | openfda.manufacturer_name | |
| ndc | package | 74307-009-01 | openfda.package_ndc |
| ndc | product | 74307-009 | openfda.product_ndc |
| ndc11 | package | 74307000901 | derived:openfda.package_ndc |
| spl id | 598025f7-a379-6780-e063-6294a90a40a0 | id | |
| spl set id | ceb71229-6c26-7ebf-e053-2a95a90ae8ad | 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.