FDA.reportPublic FDA data

Dry Spray Orignal Fresh 3.5oz

Manufacturer
BLUE SEA AEROSOL & DAILY CARE CO., LTD | BLUE SEA AEROSOL & DAILY CARE CO., LTD.
Effective date
2023-12-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:04:11

Label at a glance#

ProductDry Orignal Fresh 3.5oz
Active ingredientALUMINUM CHLOROHYDRATE
Label structure7 sections

Indications and uses

Reduces underarm wetness

Dosage and administration

For undearm 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.

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 undearm 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

Tocopheryl Acetate

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-130849607074706GTIN-13: 0849607074706
EAN-13: 0849607074706
GTIN-12: 849607074706
UPC-A: 849607074706
GTIN storage (14 digits): 00849607074706		label 1.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72119-008-012025-01-30C16284748780-12cef2736-7234-d83d-e063-dadaa90ab31fDry Spray Orignal Fresh 3.5oz

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72119-008-01Dry Orignal Fresh 3.5oz99 g in 1 CANAEROSOL, SPRAY991

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72119-008DRY ORIGNAL FRESH 3.5OZ (ALUMINUM CHLOROHYDRATE) AEROSOL, SPRAY [BLUE SEA AEROSOL & DAILY CARE CO., LTD]11 package rows20231214_0c726342-1a74-cfa0-e063-6294a90a2885.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
72119-00872119-008-01

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
DIMETHICONE92RU3N3Y1OIACT
ALKYL (C12-15) BENZOATEA9EJ3J61HQIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
DISTEARDIMONIUM HECTORITEX687XDK09LIACT
PPG-14 BUTYL ETHERR199TJT95TIACT
OCTYLDODECANOL461N1O614YIACT
CYCLOMETHICONE 50THT5PCI0RIACT
PROPANET75W9911L6IACT
ALUMINUM CHLOROHYDRATEHPN8MZW13MACTIB
BUTANE6LV4FOR43RIACT
1,1-DIFLUOROETHANE0B1U8K2ME0IACT
PROPYLENE CARBONATE8D08K3S51EIACT
SUNFLOWER OIL3W1JG795YIIACT
ISOBUTANEBXR49TP611IACT
BUTYLATED HYDROXYTOLUENE1P9D0Z171KIACT

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
0c729c2b-47c5-09d9-e063-6294a90afb010c726342-1a74-cfa0-e063-6294a90a28852023-12-14WarningsExact identifier
spl id: 0c729c2b-47c5-09d9-e063-6294a90afb01
spl set id: 0c726342-1a74-cfa0-e063-6294a90a2885

Reported adverse events (FAERS/openFDA)#

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