Dry Spray Original Fresh 3.5oz

Manufacturer: BLUE SEA AEROSOL & DAILY CARE CO., LTD.
Effective date: 2023-12-13
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 00:04:10

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

label 1

label 2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
72119-006-01	2025-01-30	C162847	48780-1	2cef2736-7eaf-d83d-e063-dadaa90ab31f	Dry Spray Original Fresh 3.5oz

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
72119-006-01	Dry Original Fresh 3.5oz	99 g in 1 CAN	AEROSOL, SPRAY	99		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72119-006	DRY ORIGINAL FRESH 3.5OZ (ALUMINUM CHLOROHYDRATE) AEROSOL, SPRAY [BLUE SEA AEROSOL & DAILY CARE CO., LTD.]	1	1 package rows	20231214_0c5f5bd8-6fa0-bb44-e063-6294a90ae830.zip

Products#

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

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

Dry Original Fresh 3.5oz
Aluminum Chlorohydrate
BUTANE
PROPYLENE CARBONATE
CYCLOMETHICONE 5
PROPANE
1,1-DIFLUOROETHANE
PPG-14 BUTYL ETHER
ALKYL (C12-15) BENZOATE
SUNFLOWER OIL
BUTYLATED HYDROXYTOLUENE
DISTEARDIMONIUM HECTORITE
ISOBUTANE
DIMETHICONE
OCTYLDODECANOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
72119-006	72119-006-01

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
Name	UNII	Kind
ALUMINUM CHLOROHYDRATE	HPN8MZW13M	ACTIB
BUTANE	6LV4FOR43R	IACT
PROPYLENE CARBONATE	8D08K3S51E	IACT
CYCLOMETHICONE 5	0THT5PCI0R	IACT
PROPANE	T75W9911L6	IACT
1,1-DIFLUOROETHANE	0B1U8K2ME0	IACT
PPG-14 BUTYL ETHER	R199TJT95T	IACT
ALKYL (C12-15) BENZOATE	A9EJ3J61HQ	IACT
SUNFLOWER OIL	3W1JG795YI	IACT
BUTYLATED HYDROXYTOLUENE	1P9D0Z171K	IACT
DISTEARDIMONIUM HECTORITE	X687XDK09L	IACT
ISOBUTANE	BXR49TP611	IACT
DIMETHICONE	92RU3N3Y1O	IACT
OCTYLDODECANOL	461N1O614Y	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
0c5f5bd8-6fa1-bb44-e063-6294a90ae830			0c5f5bd8-6fa0-bb44-e063-6294a90ae830	2023-12-13	Warnings	Exact identifier spl id: 0c5f5bd8-6fa1-bb44-e063-6294a90ae830 spl set id: 0c5f5bd8-6fa0-bb44-e063-6294a90ae830

Reported adverse events (FAERS/openFDA)#

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