FDA.reportPublic FDA data

Antiperspirant Deodorant Ultra Fresh 2oz

Manufacturer
Rejoice International Corp. | China Ningbo Shangge Cosmetics Technology Corp.
Effective date
2025-05-28
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:01:39

Label at a glance#

ProductAntiperspirant Deodorant Ultra Fresh 2oz
Active ingredientALUMINUM CHLOROHYDRATE
Label structure7 sections

Dosage and administration

Remove cap. Turn dial to raise product. Apply evenly to underarm only. Replace cap after use.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum Chlorohydrate 19%

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Use

INDICATIONS & USAGE SECTION

Reduces underarm wetness and perspiration.

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

Do not use on broken or irritated skin.

Stop use and ask a doctor if

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash develops.

Ask a doctor before use if

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have kidney disease.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, seek medical help or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Remove cap. Turn dial to raise product. Apply evenly to underarm only. Replace cap after use.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Mineral Oil

Cetearyl Alcohol

Talc

Cyclopentasiloxane

Isopropyl Myristate

Hydrogenated Castor Oil

Petrolatum

Corn Starch Modified

Fragrance

Sodium Bicarbonate

label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labelabe

labellabel

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
fb7ab793-2c12-4079-b100-a64f73bef25aProduct name420240712
b0cbf770-6cc3-4aa4-9158-755110c2b9f7Product name220230717
dc7c5daa-021f-40dd-b00d-63982cb2067aProduct name120230426
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name520200925
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name220160823
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
57337-173-01Antiperspirant Deodorant Ultra Fresh 2oz57 g in 1 BOTTLESTICK572
57337-173-02Antiperspirant Deodorant Ultra Fresh 2oz45 g in 1 BOTTLESTICK452

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
57337-17357337-173-01, 57337-173-02

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
TALC7SEV7J4R1UIACT
SODIUM BICARBONATE8MDF5V39QOIACT
ALUMINUM CHLOROHYDRATEHPN8MZW13MACTIB
MINERAL OILT5L8T28FGPIACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
STARCH, CORNO8232NY3SJIACT
PETROLATUM4T6H12BN9UIACT
HYDROGENATED CASTOR OILZF94AP8MEYIACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
CYCLOMETHICONE 50THT5PCI0RIACT

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 Deodorant Ultra Fresh 2ozALUMINUM CHLOROHYDRATERejoice International Corp.23a1e6db-ec2f-98f1-e063-6394a90a099f2025-05-28WarningsExact identifier
ndc (package): 57337-173-01
ndc (package): 57337-173-02
ndc (product): 57337-173
ndc11 (package): 57337017302
ndc11 (package): 57337017301
spl id: 363c635d-0212-071a-e063-6294a90aba6a
spl set id: 23a1e6db-ec2f-98f1-e063-6394a90a099f

Reported adverse events (FAERS/openFDA)#

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