warnings
For external use only. Do not use on broken or irritated skin Stop use and ask a doctor if rash or irritation occurs Ask a doctor before use if you have kidney disease
Carpe Antiperspirant Amber Glow
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
- Carpe Antiperspirant Amber Glow
- Generic name
- ALUMINUM. SESQUICHLOROHYDRATE
- Manufacturer
- Clutch Inc
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 3ec4f161-78c6-6bcf-e063-6394a90aa4f6
- SPL ID
- 597f48e3-8739-4606-e063-6394a90a2092
- Version
- 4
- Effective date
- 2026-08-20
- Source export date
- 2026-10-30
- 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/2026-10-30/9abf0f8b126f8aad070e21ea702bfb5e39ce670b16ae57dd52e8877705d1bf5d/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
- Import run
- 20261102T182004Z
- Imported at
- 2026-11-02 19:29:54
| 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 | Carpe Antiperspirant Amber Glow | openfda.brand_name | |
| generic name | ALUMINUM. SESQUICHLOROHYDRATE | openfda.generic_name | |
| manufacturer name | Clutch Inc | openfda.manufacturer_name | |
| ndc | package | 74307-161-01 | openfda.package_ndc |
| ndc | product | 74307-161 | openfda.product_ndc |
| ndc11 | package | 74307016101 | derived:openfda.package_ndc |
| spl id | 597f48e3-8739-4606-e063-6394a90a2092 | id | |
| spl set id | 3ec4f161-78c6-6bcf-e063-6394a90aa4f6 | set_id | |
| unii | UCN889409V | 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.