Dry Spray Original Fresh 3.5oz

Manufacturer
Rejoice International Corp. | BLUE SEA AEROSOL & DAILY CARE CO., LTD.
Effective date
2025-02-06
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:54:33

Label at a glance#

ProductDry Original Fresh 3.5oz
Active ingredientALUMINUM CHLOROHYDRATE
Label structure7 sections

Indications and uses

Reduces underarm wetness

Dosage and administration

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

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum Chlorohydrate 20.2%

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Uses

INDICATIONS & USAGE SECTION

Reduces underarm wetness

Warnings

WARNINGS SECTION

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

Do not use

OTC - DO NOT USE SECTION

Do not use on broken or irritated skin. Stop use if rash or irritation develops.

When using

OTC - WHEN USING SECTION

  • 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 120ºF/50ºC or enclosed places that could overheat.
  • USE ONLY AS DIRECTED. INTENTIONAL MISUSE BY DELIBERATELY CONCENTRATING AND INHALING THE CONTENT CAN BE HARMFUL OR FATAL.

Ask a doctor

OTC - ASK DOCTOR SECTION

Ask a doctor before using, if you have kidney disease.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

Directions

DOSAGE & ADMINISTRATION SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Cyclopentasiloxane; Butane; Propane; Isobutane; Hydrofluorocarbon 152A; PPG-14 Butyl Ether; C12-15 Alkyl Benzoate; Helianthus Annuus (Sunflower) Seed Oil; Fragrance; BHT; Dimethiconol; Disteardimonium Hectorite; Octldodecanol; Propylene Carbonate

label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
57337-158-012025-02-06C16284748780-12cef2736-7fe6-d83d-e063-dadaa90ab31fDry Spray Original Fresh 3.5oz
57337-158-012025-01-30C16284748780-12cef2736-7fe6-d83d-e063-dadaa90ab31fDry Spray Original Fresh 3.5oz

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
57337-158-01Dry Original Fresh 3.5oz99 g in 1 CANAEROSOL, SPRAY992

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
57337-158DRY ORIGINAL FRESH 3.5OZ (ALUMINUM CHLOROHYDRATE) AEROSOL, SPRAY [REJOICE INTERNATIONAL CORP.]2Current NDC, 1 package rows20250209_0c5dfbec-3ccc-5d19-e063-6394a90a956c.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
57337-15857337-158-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 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
Dry Original Fresh 3.5ozALUMINUM CHLOROHYDRATERejoice International Corp.0c5dfbec-3ccc-5d19-e063-6394a90a956c2025-02-06WarningsExact identifier
ndc (package): 57337-158-01
ndc (product): 57337-158
ndc11 (package): 57337015801
spl id: 2d769e47-7f00-d8aa-e063-6294a90a6dc0
spl set id: 0c5dfbec-3ccc-5d19-e063-6394a90a956c

Reported adverse events (FAERS/openFDA)#

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