FDA.reportPublic FDA data

Dry Spray Shower Fresh 3.5oz

Manufacturer
BLUE SEA AEROSOL & DAILY CARE CO., LTD.
Effective date
2023-12-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:04:46

Label at a glance#

ProductDry Shower 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 23.3%

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; Fragrance; BHT; Caprylic/Capric Triglyceride; Disteardimonium Hectorite; Propylene Carbonate; Sodium Starch Octenylsuccinate; Hydrolyzed Corn Starch; Silica; Corn Starch/Maltodextrin Crosspolymer; Hydrated Silica; Sodium Benzoate; Gelatin Crosspolymer; Cellulose Gum

label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label 1label 1

label 2label 2

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130849607074720GTIN-13: 0849607074720
EAN-13: 0849607074720
GTIN-12: 849607074720
UPC-A: 849607074720
GTIN storage (14 digits): 00849607074720		label 1.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72119-010-012025-01-30C16284748780-12cef2736-6817-d83d-e063-dadaa90ab31fDry Spray Shower Fresh 3.5oz

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72119-010-01Dry Shower Fresh 3.5oz99 g in 1 CANAEROSOL, SPRAY991

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72119-010DRY SHOWER FRESH 3.5OZ (ALUMINUM CHLOROHYDRATE) AEROSOL, SPRAY [BLUE SEA AEROSOL & DAILY CARE CO., LTD.]11 package rows20231218_0cbfe47f-ddfc-4291-e063-6394a90adacd.zip

Products#

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

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72119-01072119-010-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 19 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALUMINUM STARCH OCTENYLSUCCINATEI9PJ0O6294IACT
GELATIN, UNSPECIFIED2G86QN327LIACT
PPG-14 BUTYL ETHERR199TJT95TIACT
BUTYLATED HYDROXYTOLUENE1P9D0Z171KIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
STARCH, CORNO8232NY3SJIACT
1,1-DIFLUOROETHANE0B1U8K2ME0IACT
ALUMINUM CHLOROHYDRATEHPN8MZW13MACTIB
ISOBUTANEBXR49TP611IACT
HYDRATED SILICAY6O7T4G8P9IACT
CYCLOMETHICONE 50THT5PCI0RIACT
BUTANE6LV4FOR43RIACT
PROPANET75W9911L6IACT
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
SODIUM BENZOATEOJ245FE5EUIACT
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORMK679OBS311IACT
PROPYLENE CARBONATE8D08K3S51EIACT
DISTEARDIMONIUM HECTORITEX687XDK09LIACT
CORN SYRUP9G5L16BK6NIACT

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
0cbfe8e3-0672-42a4-e063-6394a90a9ea20cbfe47f-ddfc-4291-e063-6394a90adacd2023-12-18WarningsExact identifier
spl id: 0cbfe8e3-0672-42a4-e063-6394a90a9ea2
spl set id: 0cbfe47f-ddfc-4291-e063-6394a90adacd

Reported adverse events (FAERS/openFDA)#

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