Antiperspirant Dry Spray 1.6 oz Men

Manufacturer
Rejoice International Inc | BLUE SEA AEROSOL & DAILY CARE CO., LTD.
Effective date
2025-02-13
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 00:55:15

Label at a glance#

ProductAntiperspirant Dry 1.6 oz Men Antiperspirant
Active ingredientALUMINUM CHLOROHYDRATE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient ........................................................................... Purpose

Aluminum Chlorohydrate 23.3% .................................................. Antiperspirant

OTC - PURPOSE SECTION

Antiperspirant

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

INDICATIONS & USAGE SECTION

Reduces underarm wetness

WARNINGS SECTION

Warnings

For external use only.

Flammable. Do not use while smoking or near heat or flame or while smoking. Can cause serious injury or death.

  • Keep away from face and mouth to avoid breathing in.
  • Avoid spraying in eyes. CONTENTS UNDER PRESSURE. Do not puncture or incinerate. Do not expose to heat or store at temperatures above 120 oF/50 oC or in enclosed places that could overheat.
  • Do not use on broken skin.
  • Ask a doctor before using, if you have kidney disease
  • When using this product.
  • Keep away from face and mouth to avoid breathing it
  • avoid spraying in eyes
  • USE ONLY AS DIRECTED. INTENTIONAL MISSUSE BY DELIBERATELY CONCENTRATING AND INHAILING THE CONTENTS CAN BE HARMFUL OR FATAL.
  • Stop use if rash or irritation occurs

DOSAGE & ADMINISTRATION SECTION

Directions

  • For underarm use only. Shake can well before each use. Hold can 6 inches away from skin. Spray underarm and spray

INACTIVE INGREDIENT SECTION

Inactive Ingredients

Isobutane, Butane, Hydrofluorocarbon 152a, Cyclopentasiloxane, Alcohol, PPG-14 Butyl Ether, Helianthus Annuus Seed Oil, Isopropryl Myristate, C12-15 Alkyl Benzoate, Frangrance, Propane, Aluminum Starch Ocetenylsuccinate, Disteardimonium Hectorite, Dimethicone, Tocopheryl Acetate, BHT, Bentonite, Lauryl Phosphate

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
57337-109-012024-02-28C16284748780-1e4f33bdf-b259-d8a0-e053-dadaa90a6e4eAntiperspirant Dry Spray 1.6 oz Men
57337-109-012022-07-29C16284748780-1e4f33bdf-b259-d8a0-e053-dadaa90a6e4eAntiperspirant Dry Spray 1.6 oz Men

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
57337-109-01Antiperspirant Dry 1.6 oz MenAntiperspirant45 g in 1 BOTTLE, SPRAYAEROSOL, SPRAY454

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
57337-109ANTIPERSPIRANT DRY 1.6 OZ MEN ANTIPERSPIRANT (ALUMINUM CHLOROHYDRATE) AEROSOL, SPRAY [REJOICE INTERNATIONAL INC]4Current NDC, Legacy NDC, 1 package rows20250215_a1b3c869-2725-7501-e053-2a95a90a19f1.zip

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
57337-10957337-109-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 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
Antiperspirant Dry 1.6 oz Men AntiperspirantALUMINUM CHLOROHYDRATERejoice International Inca1b3c869-2725-7501-e053-2a95a90a19f12025-02-13WarningsExact identifier
ndc (package): 57337-109-01
ndc (product): 57337-109
ndc11 (package): 57337010901
spl id: 2e010044-3def-3a65-e063-6294a90a65a9
spl set id: a1b3c869-2725-7501-e053-2a95a90a19f1

Reported adverse events (FAERS/openFDA)#

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