Every Man Jack Sea Salt Antiperspirant

Manufacturer
RNA PHARMA, LLC
Effective date
2025-08-06
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 Sea Salt Antiperspirant
Active ingredientALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

active ingredientactive ingredient

INACTIVE INGREDIENT SECTION

inactive ingredientinactive ingredient

OTC - PURPOSE SECTION

purposepurpose

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of childrenkeep out of reach of children

INDICATIONS & USAGE SECTION

indications and usageindications and usage

WARNINGS SECTION

warningswarnings

DOSAGE & ADMINISTRATION SECTION

dosage and administrationdosage and administration

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

principal displayprincipal display

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
60717-646-73Every Man Jack Sea Salt Antiperspirant1 g in 1 CANISTERSTICK11

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
60717-64660717-646-73

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Source Document#

Source XML

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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Every Man Jack Sea Salt AntiperspirantALUMINUM ZIRCONIUM TRICHLOROHYDREX GLYRNA PHARMA, LLC3bb3ede9-015e-9eae-e063-6394a90ad8842025-08-06WarningsExact identifier
ndc (package): 60717-646-73
ndc (product): 60717-646
ndc11 (package): 60717064673
spl id: 3bb3ede9-015f-9eae-e063-6394a90ad884
spl set id: 3bb3ede9-015e-9eae-e063-6394a90ad884

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.