Every Man Jack Sandalwood Antiperspirant
- Manufacturer
- RNA PHARMA,LLC | RNA PHARMA, LLC
- Effective date
- 2025-08-05
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-06-01 01:09:27
Label at a glance#
ProductEvery Man Jack Sandalwood Antiperspirant
Active ingredientALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY
Label structure8 sections
Label contents#
Full prescribing information#
INACTIVE INGREDIENT SECTION
OTC - PURPOSE SECTION
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
INDICATIONS & USAGE SECTION
WARNINGS SECTION
DOSAGE & ADMINISTRATION SECTION
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 60717-647-73 | Every Man Jack Sandalwood Antiperspirant | 1 g in 1 CANISTER | STICK | 1 | 1 |
Products#
Every source-derived product name is available through these pages.
- Every Man Jack Sandalwood Antiperspirant
- Aluminum Zirconium Trichlorohydrex GLY
- C13-15 ALKANE
- STEARYL ALCOHOL
- ALUMINUM STARCH OCTENYLSUCCINATE
- CETYL ALCOHOL
- HYDROGENATED CASTOR OIL
- ALKYL (C12-15) BENZOATE
- JOJOBA OIL
- SILICA
- DODECAMETHYLPENTASILOXANE
- DIMETHICONE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 60717-647 | 60717-647-73 |
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 |
|---|---|---|---|---|---|---|
| Every Man Jack Sandalwood Antiperspirant | ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY | RNA PHARMA,LLC | 3ba3d826-9758-ec95-e063-6394a90a51bf | 2025-08-05 | Warnings | 60717-647-73 60717-647 60717064773 3ba3d826-9759-ec95-e063-6394a90a51bf 3ba3d826-9758-ec95-e063-6394a90a51bf |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.







