FDA.reportPublic FDA data

Antiperspirant Dry 2 oz Men

Manufacturer
Rejoice International Inc | Zhejiang Ludao Cosmetics Co., Ltd.
Effective date
2019-09-13
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:00:21

Label at a glance#

ProductAntiperspirant Dry 2 oz Men
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 immediately. Do not use on children under 2 years of age unless directed by a doctor.

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 or irrated skin. Stop use if rash or irritation develops.
  • Ask a doctor before using, if you have kidney disease.
  • KEEP OUT OF REACH OF CHILDREN.
  • USE ONLY AS DIRECTED. INTENTIONAL MISSUSE BY DELIBERATELY CONCENTRATING AND INHAILING THE CONTENTS CAN BE HARMFUL OR FATAL. Help stop inhalation abuse. For more information visit www.inhalant.org

DOSAGE & ADMINISTRATION SECTION

Directions

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

INACTIVE INGREDIENT SECTION

Inactive Ingredients

Isobutane, Butane, Hydrofluorocarbon 152a, Cyclopentasiloxane, Ethyl 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, Silica

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANELPACKAGE LABEL.PRINCIPAL DISPLAY PANEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
57337-091-012021-01-29C16284748780-1ba0f9c33-1ea1-a910-e053-dadaa90a0b85Antiperspirant Dry 2 oz Men

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
57337-091-01Antiperspirant Dry 2 oz Men56.7 g in 1 BOTTLE, SPRAYAEROSOL, SPRAY56.73

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
57337-091ANTIPERSPIRANT DRY 2 OZ MEN (ALUMINUM CHLOROHYDRATE) AEROSOL, SPRAY [REJOICE INTERNATIONAL INC]3Legacy NDC, 1 package rows20190914_526cb1de-2982-6a3e-e054-00144ff8d46c.zip

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
57337-09157337-091-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
SILICON DIOXIDEETJ7Z6XBU4IACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
ALUMINUM STARCH OCTENYLSUCCINATEI9PJ0O6294IACT
DISTEARDIMONIUM HECTORITEX687XDK09LIACT
DIMETHICONE92RU3N3Y1OIACT
ALUMINUM CHLOROHYDRATEHPN8MZW13MACTIB
CYCLOMETHICONE 50THT5PCI0RIACT
PPG-14 BUTYL ETHERR199TJT95TIACT
ALKYL (C12-15) BENZOATEA9EJ3J61HQIACT
ALCOHOL3K9958V90MIACT
BUTYLATED HYDROXYTOLUENE1P9D0Z171KIACT
ISOBUTANEBXR49TP611IACT
1,1-DIFLUOROETHANE0B1U8K2ME0IACT
SUNFLOWER OIL3W1JG795YIIACT
PROPANET75W9911L6IACT

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
9273afd7-bffe-5be8-e053-2995a90afd73526cb1de-2982-6a3e-e054-00144ff8d46c2019-09-13WarningsExact identifier
spl id: 9273afd7-bffe-5be8-e053-2995a90afd73
spl set id: 526cb1de-2982-6a3e-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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