Duke Prescott Antiperspirant
- Manufacturer
- RNA PHARMA, LLC
- Effective date
- 2024-01-17
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-06-01 00:07:27
Label at a glance#
ProductDuke Prescott Antiperspirant
Active ingredientALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY
Label structure8 sections
Label contents#
Full prescribing information#
OTC - PURPOSE SECTION
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
INDICATIONS & USAGE SECTION
INACTIVE INGREDIENT SECTION
WARNINGS SECTION
DOSAGE & ADMINISTRATION SECTION
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 60717-911-85 | Duke Prescott Antiperspirant | 1 in 1 CANISTER | STICK | 1 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Duke Prescott Antiperspirant
- Aluminum Zirconium Trichlorohydrex GLY
- CYCLOMETHICONE 5
- STEARYL ALCOHOL
- GLYCERIN
- SILICON DIOXIDE
- ALOE VERA LEAF
- HAMAMELIS VIRGINIANA LEAF
- ALUMINUM STARCH OCTENYLSUCCINATE
- POLYGLYCERIN-3
- HYDROGENATED CASTOR OIL
- DIMETHICONOL (40 CST)
- .ALPHA.-TOCOPHEROL ACETATE
- ACTIVATED CHARCOAL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 60717-911 | 60717-911-85 |
Ingredients#
Every source-derived ingredient row is available through these pages.
Source Document#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Duke Prescott Antiperspirant | ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY | RNA PHARMA, LLC | 0f2c478d-a06c-e8fa-e063-6394a90a4f51 | 2024-01-17 | Warnings | 60717-911-85 60717-911 60717091185 0f2c478d-a06d-e8fa-e063-6394a90a4f51 0f2c478d-a06c-e8fa-e063-6394a90a4f51 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.







