FDA.reportPublic FDA data

Antiperspirant Dry 1.6 oz Lady

Manufacturer
Rejoice International Inc. | BLUE SEA AEROSOL & DAILY CARE CO., LTD.
Effective date
2025-02-13
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 00:55:15

Label at a glance#

ProductAntiperspirant Dry 1.6 oz Lady 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 spray near flame or while smoking.
Contents under pressure
Do not crush, puncture or incinerate container.
Do not expose to heat or store at temperatures above 120oF
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 directed. Intentional missuse by deliberately concentrating and inhaling the contents can be harmful or fatal
Stop use if rash or irritation develops.

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

LabelLabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
57337-108-012024-02-28C16284748780-1e4f33bdf-adb0-d8a0-e053-dadaa90a6e4eAntiperspirant Dry 1.6 oz Lady
57337-108-012022-07-29C16284748780-1e4f33bdf-adb0-d8a0-e053-dadaa90a6e4eAntiperspirant Dry 1.6 oz Lady

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
57337-108-01Antiperspirant Dry 1.6 oz LadyAntiperspirant45 g in 1 BOTTLE, SPRAYAEROSOL, SPRAY455

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
57337-108ANTIPERSPIRANT DRY 1.6 OZ LADY ANTIPERSPIRANT (ALUMINUM CHLOROHYDRATE) AEROSOL, SPRAY [REJOICE INTERNATIONAL INC.]5Current NDC, Legacy NDC, 1 package rows20250215_a1b37ad3-a4d6-8d92-e053-2a95a90a7747.zip

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
57337-10857337-108-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MIACT
BUTYLATED HYDROXYTOLUENE1P9D0Z171KIACT
ISOBUTANEBXR49TP611IACT
1,1-DIFLUOROETHANE0B1U8K2ME0IACT
SUNFLOWER OIL3W1JG795YIIACT
PROPANET75W9911L6IACT
LAURYL PHOSPHATE0K08L8GE2HIACT
ALUMINUM CHLOROHYDRATEHPN8MZW13MACTIB
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
ALUMINUM STARCH OCTENYLSUCCINATEI9PJ0O6294IACT
DISTEARDIMONIUM HECTORITEX687XDK09LIACT
CYCLOMETHICONE 50THT5PCI0RIACT
PPG-14 BUTYL ETHERR199TJT95TIACT
ALKYL (C12-15) BENZOATEA9EJ3J61HQIACT

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 Lady AntiperspirantALUMINUM CHLOROHYDRATERejoice International Inc.a1b37ad3-a4d6-8d92-e053-2a95a90a77472025-02-13WarningsExact identifier
ndc (package): 57337-108-01
ndc (product): 57337-108
ndc11 (package): 57337010801
spl id: 2e00fe70-64da-f6e7-e063-6294a90a5f5e
spl set id: a1b37ad3-a4d6-8d92-e053-2a95a90a7747

Reported adverse events (FAERS/openFDA)#

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