warnings
Warnings For external use only
Kiehls Since 1851 Body Fuel Antiperspirant and Deodorant
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
- Kiehls Since 1851 Body Fuel Antiperspirant and Deodorant
- Generic name
- ALUMINUM CHLOROHYDRATE
- Manufacturer
- L'Oreal USA Products Inc
- Product type
- HUMAN OTC DRUG
- SPL set ID
- f5ef03e1-aa3b-4cc5-8734-7b912daf0c79
- SPL ID
- 9b92a444-cab4-4c29-a0cc-2e052079380f
- Version
- 3
- Effective date
- 2023-12-30
- Source export date
- 2026-10-12
- Source partition
- 13
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/b8dac220ac9fc8ffb4d86c6e00ece30169fc4575ca0cc92e5c9ce1a524fb0249/drug-label-0013-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 03:06:21
| 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 | Kiehls Since 1851 Body Fuel Antiperspirant and Deodorant | openfda.brand_name | |
| generic name | ALUMINUM CHLOROHYDRATE | openfda.generic_name | |
| manufacturer name | L'Oreal USA Products Inc | openfda.manufacturer_name | |
| ndc | package | 49967-639-01 | openfda.package_ndc |
| ndc | product | 49967-639 | openfda.product_ndc |
| ndc11 | package | 49967063901 | derived:openfda.package_ndc |
| spl id | 9b92a444-cab4-4c29-a0cc-2e052079380f | id | |
| spl set id | f5ef03e1-aa3b-4cc5-8734-7b912daf0c79 | 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.